Canonical Allele Identifier: PA2580152028
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1794545
ClinVar RCV Id: RCV002428802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Leu890Phe
CA354814804
NM_001184.4:c.2670A>T
CA354814806
NM_001184.4:c.2670A>C