Canonical Allele Identifier: PA916032201
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490474
ClinVar RCV Id: RCV000581716 RCV000589259 RCV001834829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser824Phe
CA382543123
NM_001351834.2:c.2471C>T