Canonical Allele Identifier: PA2741867166
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2576411
ClinVar RCV Id: RCV003322470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1893Pro
CA382547723
NM_001351834.2:c.5677T>C