Canonical Allele Identifier: PA916034121
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407669
ClinVar RCV Id: RCV000468938 RCV000572377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2301Thr
CA16613422
NM_001351834.2:c.6901G>A