Canonical Allele Identifier: PA2828206251
Gene: CCDC14 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353265.1:p.Arg460Cys
CA2578151
NM_001366336.1:c.1378C>T