Canonical Allele Identifier: PA891866037
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 45300
ClinVar RCV Id: RCV000038457 RCV000467667 RCV001813351 RCV002321512 RCV002490523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro4Leu
CA135976
NM_001318054.2:c.11C>T