Canonical Allele Identifier: PA2827324975
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075066
ClinVar RCV Id: RCV004015592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly253Ala
CA388041584
NM_001330578.2:c.758G>C