Canonical Allele Identifier: PA2825038593
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1708015
ClinVar RCV Id: RCV002287176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ser986Cys
CA388032277
NM_000053.4:c.2957C>G