Canonical Allele Identifier: PA2580205695
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2453931
ClinVar RCV Id: RCV003188066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2230Phe
CA382554898
NM_001351834.2:c.6688A>T