Canonical Allele Identifier: PA2826117151
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1503402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Leu130Phe
CA354827171
NM_001184.4:c.390A>T
CA354827173
NM_001184.4:c.390A>C