Canonical Allele Identifier: PA2825070109
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1370411
ClinVar RCV Id: RCV001899329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Pro286Leu
CA404319279
NM_000159.4:c.857C>T