Canonical Allele Identifier: PA658801502
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 529447
ClinVar RCV Id: RCV000634890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg294Leu
CA404319365
NM_000159.4:c.881G>T