Allele Registry

Canonical Allele Identifier: PA2826450143

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208705

RCV002517411

ClinVar Variation:

223052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Leu371Pro	CA16616794 NM_001257989.1:c.1112T>C