Canonical Allele Identifier: PA1139726652
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 857590
ClinVar RCV Id: RCV001063297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2132Val
CA382553348
NM_001351834.2:c.6394C>G