Canonical Allele Identifier: PA891845242
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 570256
ClinVar RCV Id: RCV000691077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val1841Ile
CA382545799
NM_000051.4:c.5521G>A