Canonical Allele Identifier: PA915955099
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188900
ClinVar RCV Id: RCV000169260 RCV002254281 RCV002453567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly979Ser
CA274098
NM_001005918.3:c.2935G>A