Canonical Allele Identifier: PA2580151980
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1792785
ClinVar RCV Id: RCV002455763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Phe846Leu
CA354815872
NM_001184.4:c.2538T>G
CA354815879
NM_001184.4:c.2538T>A
CA354815894
NM_001184.4:c.2536T>C