Canonical Allele Identifier: PA916034063
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 582959
ClinVar RCV Id: RCV000707159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His2254Pro
CA382555346
NM_001351834.2:c.6761A>C