Canonical Allele Identifier: PA2573204371
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1379534
ClinVar RCV Id: RCV001883823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile671Met
CA382537090
NM_001351834.2:c.2013A>G