Canonical Allele Identifier: PA2825568279
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215328
ClinVar RCV Id: RCV000196647 RCV001273320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Ala94Val
CA321064
NM_001113756.3:c.281C>T