Canonical Allele Identifier: PA2826117408
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1447751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Ile216Thr
CA2650740
NM_001184.4:c.647T>C