Canonical Allele Identifier: PA2499270810
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1011612
ClinVar RCV Id: RCV001309436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Val187Ala
CA378920872
NM_005343.4:c.560T>C