Canonical Allele Identifier: PA916035230
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127344
ClinVar RCV Id: RCV000115148 RCV000199503 RCV000515328 RCV000587881 RCV001355668 RCV003149792 RCV003467020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Ile68Val
CA286738
NM_001351836.2:c.202A>G