Canonical Allele Identifier: PA2741866301
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2568170
ClinVar RCV Id: RCV003297573
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn685His
CA382537459
NM_001351834.2:c.2053A>C