Canonical Allele Identifier: PA2573206406
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1503402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Leu130Phe
CA354827171
NM_001354579.2:c.390A>T
CA354827173
NM_001354579.2:c.390A>C