Canonical Allele Identifier: PA2825279276
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2159677
ClinVar RCV Id: RCV003087437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly367Asp
CA388039034
NM_001005918.3:c.1100G>A