Canonical Allele Identifier: PA121458
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 11444
ClinVar RCV Id: RCV000012197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032900.1:p.Asn238Ser
CA121455
NM_001037811.2:c.713A>G