Allele Registry

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Canonical Allele Identifier: PA2825035103

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2076107

ClinVar RCV Id: RCV002968138

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Glu2295Asp	CA382556845 NM_000051.4:c.6885A>C CA382556847 NM_000051.4:c.6885A>T