Canonical Allele Identifier: PA916034513
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2620Leu
CA382561387
NM_001351834.2:c.7858G>C