Canonical Allele Identifier: PA2827877801
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 2453557
ClinVar RCV Id: RCV003183012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Leu805Phe
CA354815397
NM_001354579.2:c.2415G>T
CA354815399
NM_001354579.2:c.2415G>C