Canonical Allele Identifier: PA2827325726
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2060746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu641Val
CA250060805
NM_001330578.2:c.1921T>G