Canonical Allele Identifier: PA2825033009
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3220968
ClinVar RCV Id: RCV004515845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1356Ile
CA382528111
NM_000051.4:c.4067A>T