Canonical Allele Identifier: PA2827330374
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157955
ClinVar RCV Id: RCV000145280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1257Ser
CA271177
NM_001330579.2:c.3769G>A