Canonical Allele Identifier: PA916009074
Gene: GCDH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly178Glu
CA274254
NM_013976.3:c.533G>A