Canonical Allele Identifier: PA2825070143
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2138250
ClinVar RCV Id: RCV003050530 RCV003479465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val301Met
CA9234544
NM_000159.4:c.901G>A