Allele Registry

Canonical Allele Identifier: PA2826449325

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208614

ClinVar Variation:

223018

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Ile54Met	CA16616771 NM_001257988.1:c.162C>G