Canonical Allele Identifier: PA2825030675
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 644776
ClinVar RCV Id: RCV000798766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly327Glu
CA382531144
NM_000051.4:c.980G>A