Canonical Allele Identifier: PA645505132
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 376353
ClinVar RCV Id: RCV000424502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn2875His
CA16602795
NM_000051.4:c.8623A>C