ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826240136
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000171385
RCV003317125
RCV003765072
RCV003987413
ClinVar Variation:
191199
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001186221.1:p.Asn158Asp
CA236237
NM_001199292.2:c.472A>G