Canonical Allele Identifier: PA274777
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 191374
ClinVar RCV Id: RCV000171557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Pro286Ser
CA274776
NM_000159.4:c.856C>T