Canonical Allele Identifier: PA916033413
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127403
ClinVar RCV Id: RCV000115208 RCV000168297 RCV000220146 RCV003460805
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1743Ile
CA286882
NM_001351834.2:c.5228C>T