Canonical Allele Identifier: PA2827329777
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 633070
ClinVar RCV Id: RCV000780932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Cys1016Ser
CA388028549
NM_001330579.2:c.3047G>C
CA388028574
NM_001330579.2:c.3046T>A