Canonical Allele Identifier: PA356395
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 220531
ClinVar RCV Id: RCV000206774 RCV000216900 RCV000588892 RCV001268980 RCV000763709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2168Leu
CA350774
NM_000051.4:c.6503C>T