Canonical Allele Identifier: PA916009026
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Val133Met
CA404317460
NM_013976.3:c.397G>A