Canonical Allele Identifier: PA916034254
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186904
ClinVar RCV Id: RCV000166564 RCV000205986 RCV000235284 RCV000764942 RCV001358721 RCV003468787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn2412Ser
CA196193
NM_001351834.2:c.7235A>G