Canonical Allele Identifier: PA891844920
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574923
ClinVar RCV Id: RCV000696987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys241Arg
CA228384704
NM_000051.4:c.722A>G