Canonical Allele Identifier: PA2826449316
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2169025
ClinVar RCV Id: RCV003093053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Gly46Arg
CA10321877
NM_001257988.1:c.136G>A
CA412202689
NM_001257988.1:c.136G>C