Allele Registry

Canonical Allele Identifier: PA645400138

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208684

ClinVar Variation:

223057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Ala459Pro	CA16616799 NM_001257989.1:c.1375G>C