Canonical Allele Identifier: PA2580203047
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1779005
ClinVar RCV Id: RCV002399197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met577Ile
CA382535303
NM_001351834.2:c.1731G>C
CA382535304
NM_001351834.2:c.1731G>T
CA382535305
NM_001351834.2:c.1731G>A