Allele Registry

Canonical Allele Identifier: PA2826449428

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208713

ClinVar Variation:

223032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Leu177Pro	CA16616782 NM_001257988.1:c.530T>C