Canonical Allele Identifier: PA916032614
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1097Leu
CA10579095
NM_001351834.2:c.3291C>G
CA382517261
NM_001351834.2:c.3289T>C
CA382517277
NM_001351834.2:c.3291C>A