Canonical Allele Identifier: PA658669580
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1851Phe
CA6265727
NM_000051.4:c.5551C>T