Canonical Allele Identifier: PA2579932191
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2885653
ClinVar RCV Id: RCV003626595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr74Ser
CA378924586
NM_001130442.3:c.221C>G
CA378924588
NM_001130442.3:c.220A>T