Canonical Allele Identifier: PA2741833742
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2864000
ClinVar RCV Id: RCV003763409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Arg988Leu
CA368986988
NM_001127500.3:c.2963G>T