Canonical Allele Identifier: PA2825310892
Gene: NCDN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014839.1:p.Thr335Ser
CA339344592
NM_001014839.1:c.1003A>T
CA339344594
NM_001014839.1:c.1004C>G