Canonical Allele Identifier: PA913191965
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 635010
ClinVar RCV Id: RCV000785883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Trp225Ser
CA404318576
NM_000159.4:c.674G>C