Canonical Allele Identifier: PA2825038513
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2581394
ClinVar RCV Id: RCV003331799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.His889Leu
CA388034438
NM_000053.4:c.2666A>T