Canonical Allele Identifier: PA2825035818
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827290
ClinVar RCV Id: RCV001026878 RCV001042524 RCV003467692 RCV003492211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2620Leu
CA382561387
NM_000051.4:c.7858G>C