Canonical Allele Identifier: PA2573202218
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1442772
ClinVar RCV Id: RCV001953159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1368Leu
CA382528619
NM_001351834.2:c.4102T>C
CA382528669
NM_001351834.2:c.4104T>A
CA382528673
NM_001351834.2:c.4104T>G