Canonical Allele Identifier: PA658673866
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482657
ClinVar RCV Id: RCV000798756 RCV000571763
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu651Pro
CA382536697
NM_000051.4:c.1952T>C