Canonical Allele Identifier: PA168454
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142475
ClinVar RCV Id: RCV000131609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2643Glu
CA168452
NM_000051.4:c.7927A>G