Canonical Allele Identifier: PA2826450108
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 342141
ClinVar RCV Id: RCV000283127 RCV000377624 RCV001478639 RCV001148526 RCV003957767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Phe343Cys
CA10321499
NM_001257989.1:c.1028T>G