Canonical Allele Identifier: PA2573204745
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1464137
ClinVar RCV Id: RCV001961280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser891Leu
CA382545109
NM_001351834.2:c.2672C>T