Canonical Allele Identifier: PA1139734616
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 990353
ClinVar RCV Id: RCV001278350 RCV002418872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser677Gly
CA228393641
NM_001351834.2:c.2029A>G