Canonical Allele Identifier: PA274949
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 193798
ClinVar RCV Id: RCV000173982 RCV000414299 RCV003955020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met405Val
CA274948
NM_000159.4:c.1213A>G