Allele Registry

Canonical Allele Identifier: PA2826449418

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208643

ClinVar Variation:

223030

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Ser160Pro	CA16616780 NM_001257988.1:c.478T>C