Canonical Allele Identifier: PA2573186392
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1482909
ClinVar RCV Id: RCV001995872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile991Phe
CA388028513
NM_001243182.2:c.2971A>T