Canonical Allele Identifier: PA324948
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215330
ClinVar RCV Id: RCV000676464 RCV001145863 RCV001273319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Ala134Val
CA324943
NM_001953.5:c.401C>T