Canonical Allele Identifier: PA658676684
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459948
ClinVar RCV Id: RCV000539888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu397Lys
CA404321719
NM_000159.4:c.1189G>A