Canonical Allele Identifier: PA2827326841
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074582
ClinVar RCV Id: RCV004014116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Met1096Lys
CA388026129
NM_001330578.2:c.3287T>A