Canonical Allele Identifier: PA2827326805
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074876
ClinVar RCV Id: RCV004015402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile1083Val
CA388026440
NM_001330578.2:c.3247A>G