Allele Registry

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Canonical Allele Identifier: PA2826449790

Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 902224

ClinVar RCV Id: RCV001148636

ClinVar Variation Id: 1403281

ClinVar RCV Id: RCV001898753 RCV004042571

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Gly10Arg	CA10321894 NM_001257989.1:c.28G>C CA10321895 NM_001257989.1:c.28G>A