ClinGen Allele Registry
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Canonical Allele Identifier:
PA645498513
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000410433
RCV001387756
ClinVar Variation:
371413
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000405.1:p.Asn457Asp
CA3382214
NM_000414.4:c.1369A>G