Canonical Allele Identifier: PA2825279358
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 860062
ClinVar RCV Id: RCV001066306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr433Ala
CA6989381
NM_001005918.3:c.1297A>G