Canonical Allele Identifier: PA169929
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142977
ClinVar RCV Id: RCV000132484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile190Lys
CA169927
NM_000051.4:c.569T>A