Allele Registry

Canonical Allele Identifier: PA2826450160

Gene: TYMP HGNC NCBI

ClinVar Allele:

224778

ClinVar RCV:

RCV000208644

ClinVar Variation:

223053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Ala387Thr	CA16616795 NM_001257989.1:c.1159G>A