Canonical Allele Identifier: PA916028296
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 660018
ClinVar RCV Id: RCV000817129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Asp949His
CA388030658
NM_001330578.2:c.2845G>C