Canonical Allele Identifier: PA2825038026
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3069925
ClinVar RCV Id: RCV004009957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Val374Gly
CA6989440
NM_000053.4:c.1121T>G