Canonical Allele Identifier: PA658671123
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2951Ile
CA382529526
NM_000051.4:c.8851G>A