Canonical Allele Identifier: PA645501298
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407714
ClinVar RCV Id: RCV000461440 RCV000486367 RCV002436411
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser933Thr
CA16613375
NM_000051.4:c.2797T>A