Canonical Allele Identifier: PA916032268
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407609
ClinVar RCV Id: RCV000474745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser854Pro
CA16613107
NM_001351834.2:c.2560T>C