Canonical Allele Identifier: PA2825030939
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 862189
ClinVar RCV Id: RCV001068865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu439Gln
CA382533655
NM_000051.4:c.1316T>A