Canonical Allele Identifier: PA658673485
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482726
ClinVar RCV Id: RCV000780889 RCV001549733 RCV000574948 RCV000627910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys219Arg
CA6264641
NM_000051.4:c.655T>C