Canonical Allele Identifier: PA2826450133
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2086738
ClinVar RCV Id: RCV003007635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Ser362Leu
CA412197599
NM_001257989.1:c.1085C>T