Allele Registry

Canonical Allele Identifier: PA2826450039

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208628

RCV001853325

ClinVar Variation:

223041

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.His283Asp	CA16616787 NM_001257989.1:c.847C>G