Canonical Allele Identifier: PA2580181609
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2185613
ClinVar RCV Id: RCV002632540 RCV004069068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Val424Met
CA325560333
NM_001257989.1:c.1270G>A