Canonical Allele Identifier: PA645481277
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 228479
ClinVar RCV Id: RCV000218594 RCV001668384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848018.1:p.Ser206Phe
CA2755292
NM_178335.3:c.617C>T