Canonical Allele Identifier: PA2580152501
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 2110669
ClinVar RCV Id: RCV003042459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Val1534Leu
CA354796835
NM_001184.4:c.4600G>T
CA354796836
NM_001184.4:c.4600G>C