Canonical Allele Identifier: PA2826819060
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 194706
ClinVar RCV Id: RCV000175136 RCV000224951 RCV000298832 RCV000353669 RCV000509557 RCV001084433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Ala467Thr
CA201313
NM_001292027.2:c.1399G>A