Canonical Allele Identifier: PA2741865901
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2753650
ClinVar RCV Id: RCV003500072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro444Leu
CA382533711
NM_001351834.2:c.1331C>T