Allele Registry

Canonical Allele Identifier: PA645407197

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208685

RCV004526644

ClinVar Variation:

223031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001944.1:p.Met173Arg	CA16616781 NM_001953.5:c.518T>G