Canonical Allele Identifier: PA2825621239
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 822592
ClinVar RCV Id: RCV001018062 RCV001039921 RCV003467644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Arg1005Gln
CA164905068
NM_001127500.3:c.3014G>A