Canonical Allele Identifier: PA2828206323
Gene: CCDC14 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353268.1:p.Arg499Cys
CA2578151
NM_001366339.1:c.1495C>T