Canonical Allele Identifier: PA916022186
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40448
ClinVar RCV Id: RCV000038467 RCV000234040 RCV000520658 RCV000755642 RCV002258783 RCV003944865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro95Ser
CA135994
NM_001318054.2:c.283C>T