Canonical Allele Identifier: PA091797
Gene: ATM HGNC NCBI
ClinVar RCV:
RCV000003167
ClinVar Variation:
3028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2656Pro
CA115935
NM_000051.4:c.7967T>C