Canonical Allele Identifier: PA2825030386
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2568244
ClinVar RCV Id: RCV003283565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln201His
CA382528113
NM_000051.4:c.603G>C
CA382528114
NM_000051.4:c.603G>T