ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826818847
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000493335
RCV000671323
RCV001856978
RCV002282178
RCV004541543
ClinVar Variation:
430263
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001278956.1:p.Arg224His
CA3381977
NM_001292027.2:c.671G>A