Canonical Allele Identifier: PA1139728055
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 919109
ClinVar RCV Id: RCV001177046 RCV003605734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2372Val
CA382559429
NM_001351834.2:c.7115A>T