Canonical Allele Identifier: PA2825035808
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1692966
ClinVar RCV Id: RCV002259297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2616Ile
CA382561361
NM_000051.4:c.7848G>A
CA382561362
NM_000051.4:c.7848G>C
CA382561363
NM_000051.4:c.7848G>T