Canonical Allele Identifier: PA2828323083
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11603
ClinVar RCV Id: RCV000012367 RCV000012366 RCV001857334
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356302.1:p.Ser47Arg
CA121600
NM_001369373.1:c.139A>C
CA414247028
NM_001369373.1:c.141T>A
CA414247029
NM_001369373.1:c.141T>G