Canonical Allele Identifier: PA916061628
Gene: CCDC88A HGNC NCBI

Linked Data

ClinVar Variation Id: 502048
ClinVar RCV Id: RCV000591724 RCV004024838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060554.3:p.Met1016Thr
CA1665852
NM_018084.5:c.3047T>C