Canonical Allele Identifier: PA2827330681
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075569
ClinVar RCV Id: RCV004017087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Asp1362Glu
CA388018998
NM_001330579.2:c.4086C>G
CA388018999
NM_001330579.2:c.4086C>A