Canonical Allele Identifier: PA645479955
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 370244
ClinVar RCV Id: RCV000411040 RCV001556801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Pro248Leu
CA16041971
NM_000159.4:c.743C>T