Canonical Allele Identifier: PA091814
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala1018Val
CA273886
NM_000053.4:c.3053C>T