Canonical Allele Identifier: PA2579931338
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1561537
ClinVar RCV Id: RCV002198241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gln95Arg
CA378924293
NM_001130442.3:c.284A>G