Canonical Allele Identifier: PA2573100328
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1334242
ClinVar RCV Id: RCV001813657 RCV002541490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ala59Ser
CA378924686
NM_176795.5:c.175G>T