Canonical Allele Identifier: PA2579932548
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1810343
ClinVar RCV Id: RCV003238902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala59Gly
CA378924683
NM_001130442.3:c.176C>G