Canonical Allele Identifier: PA916031334
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802725
ClinVar RCV Id: RCV000988643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser169Phe
CA382527461
NM_001351834.2:c.506C>T