Canonical Allele Identifier: PA916009029
Gene: GCDH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ser139Trp
CA404317502
NM_013976.3:c.416C>G