Canonical Allele Identifier: PA2580364800
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1706404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Pro217Leu
CA404318490
NM_013976.3:c.650C>T