Canonical Allele Identifier: PA2825036137
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2837683
ClinVar RCV Id: RCV003606565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2752Phe
CA382562674
NM_000051.4:c.8254A>T