Canonical Allele Identifier: PA2825033024
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1737660
ClinVar RCV Id: RCV002323150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1362Thr
CA382528378
NM_000051.4:c.4085G>C