Canonical Allele Identifier: PA2579930591
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40439
ClinVar RCV Id: RCV000157920 RCV000143899 RCV000524082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ile93Val
CA296061
NM_001130442.3:c.277A>G