Canonical Allele Identifier: PA157182
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133636
ClinVar RCV Id: RCV000120161 RCV000199628 RCV000131504 RCV000587628 RCV001250430 RCV003153382 RCV002492419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2691Cys
CA157180
NM_000051.4:c.8071C>T