Canonical Allele Identifier: PA916071790
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376444
ClinVar RCV Id: RCV000420757 RCV000422470 RCV000423098 RCV000424391 RCV000427302 RCV000431015 RCV000432499 RCV000432733 RCV000435578 RCV000437532 RCV000442518 RCV000444550 RCV000444619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gln61Glu
CA16602879
NM_176795.5:c.181C>G