Canonical Allele Identifier: PA645501834
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236707
ClinVar RCV Id: RCV000227875 RCV000569109 RCV000486877 RCV001030527 RCV001818551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1205His
CA6265325
NM_000051.4:c.3614G>A