Canonical Allele Identifier: PA658826413
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 554907
ClinVar RCV Id: RCV000670621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala304Thr
CA9234545
NM_000159.4:c.910G>A