Canonical Allele Identifier: PA2826317166
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Val149Met
CA6989561
NM_001243182.2:c.445G>A