Canonical Allele Identifier: PA916071771
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 391700
ClinVar RCV Id: RCV000443979 RCV002060067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gly60Val
CA16606948
NM_176795.5:c.179G>T