Canonical Allele Identifier: PA2827629865
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453356
ClinVar RCV Id: RCV000560752 RCV001185975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Val4Ala
CA382518955
NM_001351835.2:c.11T>C