Canonical Allele Identifier: PA091882
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 623152
ClinVar RCV Id: RCV000761257 RCV002286787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1149Ala
CA388026664
NM_000053.4:c.3446G>C