Canonical Allele Identifier: PA916032751
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216202
ClinVar RCV Id: RCV000195728 RCV000479830 RCV000562379 RCV001192418
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg1205Cys
CA335899
NM_001351834.2:c.3613C>T