Canonical Allele Identifier: PA2826240064
Gene: HSD17B4 HGNC NCBI
ClinVar RCV:
RCV001337531
ClinVar Variation:
1034763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Arg46Ser
CA360864466
NM_001199292.2:c.138G>C
CA360864467
NM_001199292.2:c.138G>T