Canonical Allele Identifier: PA2573063940
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1308069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ile987Val
CA6988631
NM_001005918.3:c.2959A>G