Canonical Allele Identifier: PA916032010
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile665Val
CA16613020
NM_001351834.2:c.1993A>G