Canonical Allele Identifier: PA2825279694
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1516399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr726Ser
CA388034452
NM_001005918.3:c.2177C>G
CA388034459
NM_001005918.3:c.2176A>T