Canonical Allele Identifier: PA658826411
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 554513
ClinVar RCV Id: RCV000670161 RCV001731873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Asn291Lys
CA404319333
NM_000159.4:c.873C>A
CA404319335
NM_000159.4:c.873C>G