Canonical Allele Identifier: PA2827326370
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075602
ClinVar RCV Id: RCV004017120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly920Val
CA388032104
NM_001330578.2:c.2759G>T