Allele Registry

Canonical Allele Identifier: PA2826449615

Gene: TYMP HGNC NCBI

ClinVar Allele:

224776

ClinVar RCV:

RCV000208689

ClinVar Variation:

223051

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Leu356Pro	CA16616793 NM_001257988.1:c.1067T>C