Canonical Allele Identifier: PA2827329979
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1948557
ClinVar RCV Id: RCV002667828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1106Val
CA6988635
NM_001330579.2:c.3317G>T