Canonical Allele Identifier: PA916034026
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574340
ClinVar RCV Id: RCV000696256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2224Leu
CA382554863
NM_001351834.2:c.6670A>C
CA382554864
NM_001351834.2:c.6670A>T