Canonical Allele Identifier: PA2826317743
Gene: ATP7B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Asp654Gly
CA388021872
NM_001243182.2:c.1961A>G