Canonical Allele Identifier: PA2827329941
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074582
ClinVar RCV Id: RCV004014116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Met1090Lys
CA388026129
NM_001330579.2:c.3269T>A