Canonical Allele Identifier: PA2826819086
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 226666
ClinVar RCV Id: RCV000217919 RCV000264639 RCV000359350 RCV000906457 RCV001580473 RCV004541308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Ser498Arg
CA3382309
NM_001292027.2:c.1494T>A
CA360869162
NM_001292027.2:c.1492A>C
CA360869167
NM_001292027.2:c.1494T>G