Canonical Allele Identifier: PA1139674908
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 959197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr971Ala
CA388026028
NM_001005918.3:c.2911A>G