Canonical Allele Identifier: PA658669190
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 454188
ClinVar RCV Id: RCV000532694 RCV000569043 RCV001547448 RCV000764682 RCV003470697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ala48Thr
CA4447946
NM_001127500.3:c.142G>A