Canonical Allele Identifier: PA2828526339
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575875
ClinVar RCV Id: RCV003321441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361431.1:p.Val73Leu
CA360866876
NM_001374502.1:c.217G>C
CA360866877
NM_001374502.1:c.217G>T