Canonical Allele Identifier: PA2825279778
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 554771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr786Met
CA6988850
NM_001005918.3:c.2357C>T