Canonical Allele Identifier: PA1139734768
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 955189
ClinVar RCV Id: RCV001227784 RCV003353228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser719Leu
CA382538749
NM_001351834.2:c.2156C>T