Canonical Allele Identifier: PA095527
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 371271
ClinVar RCV Id: RCV000409563
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Gly178Arg
CA9234423
NM_000159.4:c.532G>A
CA404317989
NM_000159.4:c.532G>C