Canonical Allele Identifier: PA2825030928
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1172190
ClinVar RCV Id: RCV001525857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu436Pro
CA382533627
NM_000051.4:c.1307T>C