Canonical Allele Identifier: PA215668
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 41630
ClinVar RCV Id: RCV000034535 RCV000123136 RCV000599960 RCV000563453 RCV001507142 RCV003944878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ser323Gly
CA215665
NM_001127500.3:c.967A>G