Canonical Allele Identifier: PA2825069938
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 522644
ClinVar RCV Id: RCV000625783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu181Gln
CA9234426
NM_000159.4:c.541G>C