Canonical Allele Identifier: PA1139730270
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 959105
ClinVar RCV Id: RCV001232393
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2730Leu
CA382562534
NM_001351834.2:c.8189A>T