Canonical Allele Identifier: PA2825280410
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075569
ClinVar RCV Id: RCV004017087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asp1239Glu
CA388018998
NM_001005918.3:c.3717C>G
CA388018999
NM_001005918.3:c.3717C>A