ClinGen Allele Registry
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Canonical Allele Identifier:
PA095288
Gene: GCDH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
187039
ClinVar RCV:
RCV000169118
RCV000725818
ClinVar Variation:
188789
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000150.1:p.Arg161Gln
CA273961
NM_000159.4:c.482G>A