Canonical Allele Identifier: PA2573204394
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1503916
ClinVar RCV Id: RCV002025806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe2799_Gln2800delinsLeuLys
CA2573146756
NM_001351834.2:c.8397_8398delinsAA