Canonical Allele Identifier: PA2827329917
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1404876
ClinVar RCV Id: RCV001903447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ser1078Pro
CA388026421
NM_001330579.2:c.3232T>C