Canonical Allele Identifier: PA2825279405
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2057940
ClinVar RCV Id: RCV002942124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ser481Pro
CA6989351
NM_001005918.3:c.1441T>C