Canonical Allele Identifier: PA1139730307
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 948181
ClinVar RCV Id: RCV001219390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2734Ile
CA382562563
NM_001351834.2:c.8202G>A
CA382562564
NM_001351834.2:c.8202G>C
CA382562565
NM_001351834.2:c.8202G>T