Canonical Allele Identifier: PA916032405
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu942Phe
CA197400
NM_001351834.2:c.2824C>T