Canonical Allele Identifier: PA2826117170
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1738014
ClinVar RCV Id: RCV002323504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Lys137Asn
CA354827080
NM_001184.4:c.411G>T
CA354827082
NM_001184.4:c.411G>C