Canonical Allele Identifier: PA645475338
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376322
ClinVar RCV Id: RCV000417619 RCV000419094 RCV000420448 RCV000428741 RCV000428681 RCV000435275 RCV000430658 RCV000435915 RCV000440764 RCV000424105 RCV000425877 RCV000430030 RCV000435489 RCV000441832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gln61Pro
CA16602768
NM_005343.4:c.182A>C