Canonical Allele Identifier: PA916033808
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro2056Leu
CA382550667
NM_001351834.2:c.6167C>T