Allele Registry

Canonical Allele Identifier: PA126788

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018143

RCV000199543

ClinVar Variation:

16663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Val208Met	CA126784 NM_001257988.1:c.622G>A