Canonical Allele Identifier: PA916032084
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453406
ClinVar RCV Id: RCV000566119 RCV000552619 RCV000588042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly724Ser
CA228397341
NM_001351834.2:c.2170G>A