Canonical Allele Identifier: PA916032949
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1363Ser
CA382528434
NM_001351834.2:c.4087A>T
CA382528447
NM_001351834.2:c.4088C>G