Canonical Allele Identifier: PA2825038500
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075609
ClinVar RCV Id: RCV004017127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ile873Val
CA388034791
NM_000053.4:c.2617A>G