Allele Registry

Canonical Allele Identifier: PA2826449423

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208685

RCV004526644

ClinVar Variation:

223031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Met173Arg	CA16616781 NM_001257988.1:c.518T>G