Canonical Allele Identifier: PA2741912255
Gene: HSD17B10 HGNC NCBI
ClinVar RCV:
RCV003565805
ClinVar Variation:
2744815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Glu48Ala
CA413154301
NM_004493.3:c.143A>C