Canonical Allele Identifier: PA2579933323
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 665374
ClinVar RCV Id: RCV000823640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asp92Ala
CA378924344
NM_001130442.3:c.275A>C