Canonical Allele Identifier: PA658673546
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481079
ClinVar RCV Id: RCV000570159 RCV000627865 RCV003328603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu282Phe
CA6264684
NM_000051.4:c.846A>T
CA382529470
NM_000051.4:c.846A>C