Canonical Allele Identifier: PA2826449394
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2418704
ClinVar RCV Id: RCV003121453
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Lys124Asn
CA412201987
NM_001257988.1:c.372G>T
CA412201988
NM_001257988.1:c.372G>C