Canonical Allele Identifier: PA916028275
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495404
ClinVar RCV Id: RCV000587250 RCV001003423 RCV001001851 RCV002530885 RCV003905504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Met665Val
CA6989142
NM_001330578.2:c.1993A>G