Canonical Allele Identifier: PA2825280024
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074582
ClinVar RCV Id: RCV004014116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Met967Lys
CA388026129
NM_001005918.3:c.2900T>A