Canonical Allele Identifier: PA645479897
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 235857
ClinVar RCV Id: RCV000224005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ile152Met
CA10581471
NM_000159.4:c.456C>G