Canonical Allele Identifier: PA1139730174
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 944244
ClinVar RCV Id: RCV001214602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2714Arg
CA382562238
NM_001351834.2:c.8141A>G