Canonical Allele Identifier: PA2826317265
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312396
ClinVar RCV Id: RCV000313711 RCV000425182 RCV001269200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Glu247Gly
CA6989506
NM_001243182.2:c.740A>G