Canonical Allele Identifier: PA658740687
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1363Ser
CA382528434
NM_000051.4:c.4087A>T
CA382528447
NM_000051.4:c.4088C>G