Canonical Allele Identifier: PA2579933177
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40438
ClinVar RCV Id: RCV000207497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ser89Cys
CA351483
NM_001130442.3:c.266C>G