Canonical Allele Identifier: PA916033493
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453578
ClinVar RCV Id: RCV000544492 RCV002350158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1815Asn
CA228388428
NM_001351834.2:c.5443G>A