ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916009029
Gene: GCDH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
549092
ClinVar RCV:
RCV000665802
ClinVar Variation:
550912
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_039663.1:p.Ser139Trp
CA404317502
NM_013976.3:c.416C>G