Canonical Allele Identifier: PA2573255990
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1683830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Phe236Leu
CA9234467
NM_013976.3:c.706T>C
CA404318696
NM_013976.3:c.708C>A
CA404318697
NM_013976.3:c.708C>G