Canonical Allele Identifier: PA2825031441
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1037709
ClinVar RCV Id: RCV001340902
ClinVar Variation Id: 1783809
ClinVar RCV Id: RCV002423681 RCV003605843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met660Ile
CA382536872
NM_000051.4:c.1980G>A
CA382536874
NM_000051.4:c.1980G>C
CA382536878
NM_000051.4:c.1980G>T