Allele Registry

Canonical Allele Identifier: PA2825568132

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208684

ClinVar Variation:

223057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Ala454Pro	CA16616799 NM_001113755.3:c.1360G>C