Allele Registry

Canonical Allele Identifier: PA2826449449

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208641

ClinVar Variation:

223033

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Arg202Lys	CA10321689 NM_001257988.1:c.605G>A