Canonical Allele Identifier: PA2825031612
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1474136
ClinVar RCV Id: RCV001969703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu737Lys
CA382539035
NM_000051.4:c.2209G>A