Canonical Allele Identifier: PA2825038606
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2093508
ClinVar RCV Id: RCV002996807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Met996Val
CA388032164
NM_000053.4:c.2986A>G