Canonical Allele Identifier: PA2825070250
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 656532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met366Ile
CA404321257
NM_000159.4:c.1098G>A
CA404321258
NM_000159.4:c.1098G>C
CA404321259
NM_000159.4:c.1098G>T