Canonical Allele Identifier: PA916032812
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1250Tyr
CA382524188
NM_001351834.2:c.3749C>A