Canonical Allele Identifier: PA2825035995
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 938483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2699Leu
CA382562092
NM_000051.4:c.8096C>T