Canonical Allele Identifier: PA2825035148
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2054927
ClinVar RCV Id: RCV002933076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2312His
CA382557203
NM_000051.4:c.6935T>A