Canonical Allele Identifier: PA916071782
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376033
ClinVar RCV Id: RCV000421974 RCV000420623 RCV000428206 RCV000426826 RCV000425694 RCV000428443 RCV000436845 RCV000437079 RCV000420395 RCV000433098 RCV000421690 RCV000445204 RCV000445166 RCV000430634 RCV000438263 RCV000438465 RCV000439626 RCV001372584 RCV001255684 RCV001849368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gln61Leu
CA16602500
NM_176795.5:c.182A>T
CA645569137
NM_176795.5:c.182_183delinsTA