Canonical Allele Identifier: PA2826118973
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 3221096
ClinVar RCV Id: RCV004507952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Ala901Val
CA354814669
NM_001184.4:c.2702C>T