Canonical Allele Identifier: PA916033018
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1431Ser
CA16613045
NM_001351834.2:c.4292A>G