Canonical Allele Identifier: PA891845266
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 567885
ClinVar RCV Id: RCV000688084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1896Val
CA382547762
NM_000051.4:c.5686T>G