Canonical Allele Identifier: PA2827326035
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157939
ClinVar RCV Id: RCV000145263 RCV000413599 RCV000623574 RCV003415974
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly791Arg
CA271172
NM_001330578.2:c.2371G>A
CA388034842
NM_001330578.2:c.2371G>C