Canonical Allele Identifier: PA2827329013
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 664367
ClinVar RCV Id: RCV000822452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Leu696Val
CA388020478
NM_001330579.2:c.2086C>G