Allele Registry

Canonical Allele Identifier: PA2826449863

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208657

RCV003479061

ClinVar Variation:

223019

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Met76Ile	CA16616772 NM_001257989.1:c.228G>A CA412202345 NM_001257989.1:c.228G>T CA412202346 NM_001257989.1:c.228G>C