Canonical Allele Identifier: PA2826317662
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 156281
ClinVar RCV Id: RCV000144365 RCV000497757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly599Ser
CA270731
NM_001243182.2:c.1795G>A