Canonical Allele Identifier: PA2827329262
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1516399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr804Ser
CA388034452
NM_001330579.2:c.2411C>G
CA388034459
NM_001330579.2:c.2410A>T