Canonical Allele Identifier: PA916032944
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 185171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1360Asn
CA191224
NM_001351834.2:c.4079G>A