Canonical Allele Identifier: PA2825279695
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 642900
ClinVar RCV Id: RCV000796453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr726Pro
CA388034454
NM_001005918.3:c.2176A>C