Canonical Allele Identifier: PA2573181383
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1520569
ClinVar RCV Id: RCV002030834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Gln978His
CA368986795
NM_001127500.3:c.2934A>C
CA368986797
NM_001127500.3:c.2934A>T