Canonical Allele Identifier: PA645497905
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys70Asn
CA16619095
NM_000051.4:c.210A>T
CA382521298
NM_000051.4:c.210A>C