Canonical Allele Identifier: PA2825034181
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1494842
ClinVar RCV Id: RCV001999025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu1892Asp
CA382547721
NM_000051.4:c.5676G>C
CA382547722
NM_000051.4:c.5676G>T