Canonical Allele Identifier: PA2825035786
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2067596
ClinVar RCV Id: RCV002966530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn2603Lys
CA382561278
NM_000051.4:c.7809T>A
CA382561279
NM_000051.4:c.7809T>G