Canonical Allele Identifier: PA916032934
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 577684
ClinVar RCV Id: RCV000700501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1354Gln
CA382528056
NM_001351834.2:c.4061C>A