Canonical Allele Identifier: PA356433
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 221187
ClinVar RCV Id: RCV000206872 RCV000217962 RCV001030526 RCV001174579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro960His
CA350856
NM_000051.4:c.2879C>A