Canonical Allele Identifier: PA160419
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 41624
ClinVar RCV Id: RCV000034529 RCV000121340 RCV000123120 RCV000163261 RCV000203290 RCV000431770 RCV000421063 RCV001507182 RCV002227927 RCV003891465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr1010Ile
CA160417
NM_001127500.3:c.3029C>T