Canonical Allele Identifier: PA1139734573
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 942615
ClinVar RCV Id: RCV001212636 RCV001760186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp658His
CA382536834
NM_001351834.2:c.1972G>C