Canonical Allele Identifier: PA1139748180
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 842180
ClinVar RCV Id: RCV001044559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Val45Ile
CA378924778
NM_176795.5:c.133G>A