Canonical Allele Identifier: PA2825034724
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_000042.3:p.Leu2132Val
CA382553348
NM_000051.4:c.6394C>G