Allele Registry

Canonical Allele Identifier: PA289131

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000118807

RCV000323507

RCV000403000

RCV000676456

RCV001274279

ClinVar Variation:

130693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Ser471Leu	CA289128 NM_001257988.1:c.1412C>T