Canonical Allele Identifier: PA916034537
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234186
ClinVar RCV Id: RCV000214199 RCV000538011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2634Val
CA10579273
NM_001351834.2:c.7901A>T