Canonical Allele Identifier: PA916009077
Gene: GCDH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly178Arg
CA9234423
NM_013976.3:c.532G>A
CA404317989
NM_013976.3:c.532G>C