Canonical Allele Identifier: PA645447811
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411891
ClinVar RCV Id: RCV000472256 RCV001013640 RCV001312213 RCV003225728 RCV002481472
ClinVar Variation Id: 1782924
ClinVar RCV Id: RCV002410957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Gly645Arg
CA4448325
NM_001127500.3:c.1933G>A
CA368979437
NM_001127500.3:c.1933G>C