Canonical Allele Identifier: PA1139729781
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 941254
ClinVar RCV Id: RCV001211001 RCV002418717
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn2632Lys
CA382561466
NM_001351834.2:c.7896C>A
CA382561467
NM_001351834.2:c.7896C>G