Canonical Allele Identifier: PA095229
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 285973
ClinVar RCV Id: RCV000672042 RCV000327109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala421Thr
CA9234692
NM_000159.4:c.1261G>A