Canonical Allele Identifier: PA2826318172
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312383
ClinVar RCV Id: RCV000506750 RCV000395391 RCV002321983 RCV001558379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly950Glu
CA6988785
NM_001243182.2:c.2849G>A