Canonical Allele Identifier: PA2825280409
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073899
ClinVar RCV Id: RCV004012441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asp1239Gly
CA6988416
NM_001005918.3:c.3716A>G