Canonical Allele Identifier: PA2825036498
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2575316
ClinVar RCV Id: RCV003320505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2900Val
CA382523677
NM_000051.4:c.8698C>G