Canonical Allele Identifier: PA2580206519
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2067596
ClinVar RCV Id: RCV002966530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn2603Lys
CA382561278
NM_001351834.2:c.7809T>A
CA382561279
NM_001351834.2:c.7809T>G