Canonical Allele Identifier: PA2825035691
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2723930
ClinVar RCV Id: RCV003501501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2560Arg
CA382560994
NM_000051.4:c.7679T>G