Canonical Allele Identifier: PA2499251069
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1037724
ClinVar Variation Id: 1057086
ClinVar RCV Id: RCV001366005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met855Ile
CA382543817
NM_001351834.2:c.2565G>A
CA382543819
NM_001351834.2:c.2565G>C
CA382543822
NM_001351834.2:c.2565G>T