Canonical Allele Identifier: PA645503721
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2253Asn
CA16613416
NM_000051.4:c.6759A>C
CA382555329
NM_000051.4:c.6759A>T