Canonical Allele Identifier: PA645501203
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu888Gln
CA16619144
NM_000051.4:c.2662G>C