Canonical Allele Identifier: PA916032005
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp661Asn
CA228393576
NM_001351834.2:c.1981G>A