Canonical Allele Identifier: PA658806770
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 522644
ClinVar RCV Id: RCV000625783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Glu181Gln
CA9234426
NM_013976.3:c.541G>C