Canonical Allele Identifier: PA916032270
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127353
ClinVar RCV Id: RCV000115158 RCV000565873 RCV000698456 RCV002288587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met855Thr
CA286763
NM_001351834.2:c.2564T>C