Canonical Allele Identifier: PA2825036029
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1762137
ClinVar RCV Id: RCV002421342 RCV003328699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2710Asn
CA382562190
NM_000051.4:c.8130G>C
CA382562192
NM_000051.4:c.8130G>T