Canonical Allele Identifier: PA2580253025
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2200579
ClinVar RCV Id: RCV002638287
ClinVar Variation Id: 2504710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Gln370His
CA10321486
NM_001953.5:c.1110G>T
CA412197477
NM_001953.5:c.1110G>C
CA2580099975
NM_001953.5:c.1110_1111delinsTT