Canonical Allele Identifier: PA2573203843
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1355253
ClinVar RCV Id: RCV001866824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2304Asp
CA382557032
NM_001351834.2:c.6912G>C
CA382557035
NM_001351834.2:c.6912G>T