Canonical Allele Identifier: PA2825069836
Gene: GCDH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg128Leu
CA404317415
NM_000159.4:c.383G>T