Allele Registry

Canonical Allele Identifier: PA2826449454

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208663

ClinVar Variation:

223036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Val208Gly	CA16616783 NM_001257988.1:c.623T>G