Canonical Allele Identifier: PA2826318462
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189139
ClinVar RCV Id: RCV000169558 RCV001310695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Pro1162Leu
CA274408
NM_001243182.2:c.3485C>T