Canonical Allele Identifier: PA2573071148
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1331952
ClinVar RCV Id: RCV001804468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser800Pro
CA382541120
NM_001351834.2:c.2398T>C