Canonical Allele Identifier: PA2825035826
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827298
ClinVar RCV Id: RCV001026891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2623His
CA382561406
NM_000051.4:c.7868T>A