Allele Registry

Canonical Allele Identifier: PA126772

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018136

RCV000497545

RCV001831582

ClinVar Variation:

16656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Lys222Arg	CA126768 NM_001257988.1:c.665A>G