Canonical Allele Identifier: PA2825279948
Gene: ATP7B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly892Ser
CA6988744
NM_001005918.3:c.2674G>A