Canonical Allele Identifier: PA645481266
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 429860
ClinVar RCV Id: RCV000494078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848018.1:p.Arg166Ile
CA355763684
NM_178335.3:c.497G>T