Canonical Allele Identifier: PA2825038822
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 959197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1178Ala
CA388026028
NM_000053.4:c.3532A>G