Canonical Allele Identifier: PA2825038651
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1162227
ClinVar RCV Id: RCV001507001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Met1025Lys
CA388030705
NM_000053.4:c.3074T>A