Canonical Allele Identifier: PA095288
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188789
ClinVar RCV Id: RCV000169118 RCV000725818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg161Gln
CA273961
NM_000159.4:c.482G>A