Canonical Allele Identifier: PA1139748270
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 937347
ClinVar RCV Id: RCV001206337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Phe82Cys
CA378924502
NM_176795.5:c.245T>G