Allele Registry

Canonical Allele Identifier: PA2826449474

Gene: TYMP HGNC NCBI

ClinVar Allele:

224763

ClinVar RCV:

RCV000208618

ClinVar Variation:

223038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Phe236Ser	CA16616784 NM_001257988.1:c.707T>C