Canonical Allele Identifier: PA2826449605
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2138462
ClinVar RCV Id: RCV003050585 RCV003147815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Leu347Pro
CA412197822
NM_001257988.1:c.1040T>C