Canonical Allele Identifier: PA2580205852
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2076107
ClinVar RCV Id: RCV002968138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2295Asp
CA382556845
NM_001351834.2:c.6885A>C
CA382556847
NM_001351834.2:c.6885A>T