Canonical Allele Identifier: PA2573090260
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1304015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ile250Thr
CA404318819
NM_013976.3:c.749T>C