Canonical Allele Identifier: PA916032302
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127355
ClinVar RCV Id: RCV000115160 RCV000168041 RCV000211984 RCV000767896 RCV000858203 RCV001354304 RCV004549542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn870Asp
CA286769
NM_001351834.2:c.2608A>G