Canonical Allele Identifier: PA2499251003
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1172190
ClinVar RCV Id: RCV001525857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu436Pro
CA382533627
NM_001351834.2:c.1307T>C