Canonical Allele Identifier: PA2825033181
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1739669
ClinVar RCV Id: RCV002332006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys1440Gln
CA382531788
NM_000051.4:c.4318A>C