Allele Registry

Canonical Allele Identifier: PA2826449401

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208677

ClinVar Variation:

223025

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Leu133Pro	CA16616777 NM_001257988.1:c.398T>C