Canonical Allele Identifier: PA2827326302
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr899Met
CA220308
NM_001330578.2:c.2696C>T