Canonical Allele Identifier: PA091921
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 37122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ile1148Thr
CA259856
NM_000053.4:c.3443T>C