Canonical Allele Identifier: PA286765
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127353
ClinVar RCV Id: RCV000115158 RCV000565873 RCV000698456 RCV002288587
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met855Thr
CA286763
NM_000051.4:c.2564T>C