Canonical Allele Identifier: PA2741866840
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2777765
ClinVar RCV Id: RCV003605898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1354Ser
CA382528050
NM_001351834.2:c.4060C>T