Canonical Allele Identifier: PA2579930965
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1416167
ClinVar RCV Id: RCV001935564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gln95His
CA216882864
NM_001130442.3:c.285G>C
CA378924285
NM_001130442.3:c.285G>T