Canonical Allele Identifier: PA2741940448
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2864675
ClinVar RCV Id: RCV003602591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ala293Val
CA404319358
NM_013976.3:c.878C>T