Canonical Allele Identifier: PA2826317661
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2715663
ClinVar RCV Id: RCV003503862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Leu598Phe
CA6989103
NM_001243182.2:c.1792C>T