Canonical Allele Identifier: PA2499250957
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1171556
ClinVar RCV Id: RCV001524753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2030Leu
CA382550187
NM_001351834.2:c.6088A>C