Canonical Allele Identifier: PA2580532835
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2087469
ClinVar RCV Id: RCV003009575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ala83Thr
CA378924494
NM_176795.5:c.247G>A