Canonical Allele Identifier: PA658673971
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481144
ClinVar RCV Id: RCV000562333 RCV001821666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu726Phe
CA382538821
NM_000051.4:c.2176C>T