Canonical Allele Identifier: PA2826317802
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188814
ClinVar RCV Id: RCV000169151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Leu684Phe
CA273992
NM_001243182.2:c.2050C>T