Canonical Allele Identifier: PA2827324939
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312397
ClinVar RCV Id: RCV000354484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Arg226Trp
CA6989517
NM_001330578.2:c.676C>T