Canonical Allele Identifier: PA916071787
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376318
ClinVar RCV Id: RCV000421964 RCV000420806 RCV000423449 RCV000424686 RCV000433734 RCV000433099 RCV000434965 RCV000440259 RCV000442468 RCV000444731 RCV000589258
ClinVar Variation Id: 376319
ClinVar RCV Id: RCV000428014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gln61His
CA16602764
NM_176795.5:c.183G>T
CA16602765
NM_176795.5:c.183G>C