Canonical Allele Identifier: PA2580206661
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1761651
ClinVar RCV Id: RCV002419224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2670Asn
CA382561819
NM_001351834.2:c.8010G>C
CA382561820
NM_001351834.2:c.8010G>T