Allele Registry

Canonical Allele Identifier: PA2826449313

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV001279636

ClinVar Variation:

991427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Arg44Pro	CA412202712 NM_001257988.1:c.131G>C