Canonical Allele Identifier: PA2827326670
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 633070
ClinVar RCV Id: RCV000780932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Cys1022Ser
CA388028549
NM_001330578.2:c.3065G>C
CA388028574
NM_001330578.2:c.3064T>A