Canonical Allele Identifier: PA2825036083
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 959105
ClinVar RCV Id: RCV001232393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2730Leu
CA382562534
NM_000051.4:c.8189A>T