Canonical Allele Identifier: PA098872
Gene: KCND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 66063
ClinVar RCV Id: RCV000056300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004971.2:p.Met373Ile
CA144860
NM_004980.5:c.1119G>A
CA341661009
NM_004980.5:c.1119G>T
CA341661012
NM_004980.5:c.1119G>C