Canonical Allele Identifier: PA095637
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 198396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met191Thr
CA275381
NM_000159.4:c.572T>C