Canonical Allele Identifier: PA891845024
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 582998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn859Ser
CA382543900
NM_000051.4:c.2576A>G