Canonical Allele Identifier: PA658670618
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453713
ClinVar RCV Id: RCV000527553 RCV001180547 RCV001597153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2662Ile
CA382561767
NM_000051.4:c.7984G>A