Canonical Allele Identifier: PA2826117338
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 2561373
ClinVar RCV Id: RCV003301095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Leu196Phe
CA354826357
NM_001184.4:c.588G>T
CA354826358
NM_001184.4:c.588G>C