Canonical Allele Identifier: PA891865306
Gene: CPAMD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 375309
ClinVar RCV Id: RCV000416368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056507.3:p.Ser1404Pro
CA16044053
NM_015692.5:c.4210T>C