Allele Registry

Canonical Allele Identifier: PA2826449740

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208684

ClinVar Variation:

223057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Ala454Pro	CA16616799 NM_001257988.1:c.1360G>C