Canonical Allele Identifier: PA2827326101
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1930912
ClinVar RCV Id: RCV002631301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr816Ala
CA388034344
NM_001330578.2:c.2446A>G