Canonical Allele Identifier: PA2826449669
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3185241
ClinVar RCV Id: RCV004484092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Leu397Met
CA412197042
NM_001257988.1:c.1189C>A