Canonical Allele Identifier: PA2827330405
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1271Val
CA388020155
NM_001330579.2:c.3812G>T