Canonical Allele Identifier: PA224229
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 96556
ClinVar RCV Id: RCV000082711 RCV001350616 RCV003333026
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg214His
CA224228
NM_181426.2:c.641G>A