Canonical Allele Identifier: PA2827329507
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3064956
ClinVar RCV Id: RCV003990033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr893Lys
CA388032373
NM_001330579.2:c.2678C>A