ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826240574
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000218324
RCV000301707
RCV000361158
RCV000966445
RCV001079319
RCV002494555
ClinVar Variation:
226669
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001186221.1:p.Thr669Ile
CA3382504
NM_001199292.2:c.2006C>T