Canonical Allele Identifier: PA2580112481
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1798731
ClinVar RCV Id: RCV002435702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Val984Leu
CA368987173
NM_000245.4:c.2950G>T
CA368987178
NM_000245.4:c.2950G>C