Canonical Allele Identifier: PA2827329261
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 642900
ClinVar RCV Id: RCV000796453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr804Pro
CA388034454
NM_001330579.2:c.2410A>C