Canonical Allele Identifier: PA298158
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181924
ClinVar RCV Id: RCV000159689 RCV000205354 RCV000211974 RCV001030522 RCV001174912 RCV004551371 RCV001798544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg720His
CA298156
NM_000051.4:c.2159G>A