ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826819072
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000414223
RCV001314566
ClinVar Variation:
372681
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001278956.1:p.Asp486Asn
CA3382301
NM_001292027.2:c.1456G>A