Allele Registry

Canonical Allele Identifier: PA2825568000

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208689

ClinVar Variation:

223051

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Leu356Pro	CA16616793 NM_001113755.3:c.1067T>C