Canonical Allele Identifier: PA2826240033
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3065507
ClinVar RCV Id: RCV003990584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Phe7Leu
CA360861637
NM_001199292.2:c.19T>C
CA360861648
NM_001199292.2:c.21C>A
CA360861650
NM_001199292.2:c.21C>G