Canonical Allele Identifier: PA2827628847
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232502
ClinVar RCV Id: RCV004521178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu850Asp
CA382543708
NM_001351834.2:c.2550G>C
CA382543710
NM_001351834.2:c.2550G>T