Canonical Allele Identifier: PA2742019174
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2747523
ClinVar RCV Id: RCV003514885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Val44Ala
CA378924780
NM_176795.5:c.131T>C