Canonical Allele Identifier: PA916035127
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187275
ClinVar RCV Id: RCV000166992 RCV000168377 RCV000519260 RCV002221505 RCV003483551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Met1Thr