Canonical Allele Identifier: PA2741867706
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2788012
ClinVar RCV Id: RCV003605972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2724Glu
CA382562492
NM_001351834.2:c.8170C>G