Canonical Allele Identifier: PA916032323
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys892Asn
CA382545121
NM_001351834.2:c.2676G>C
CA382545123
NM_001351834.2:c.2676G>T