ClinGen Allele Registry
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Canonical Allele Identifier:
PA645498584
Gene: HSD17B4
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000401079
RCV002227469
RCV002518987
RCV004543107
ClinVar Variation:
287598
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000405.1:p.Leu726Val
CA3382536
NM_000414.4:c.2176C>G