Canonical Allele Identifier: PA658740667
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1341Leu
CA382527654
NM_000051.4:c.4022C>T