Canonical Allele Identifier: PA2827628689
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3236729
ClinVar RCV Id: RCV004556180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly335Arg
CA382531363
NM_001351834.2:c.1003G>A
CA382531365
NM_001351834.2:c.1003G>C