Canonical Allele Identifier: PA2573065025
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 1337020
ClinVar RCV Id: RCV001819506 RCV002542032 RCV004040976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Pro1969Leu
CA7308562
NM_001080414.4:c.5906C>T