Canonical Allele Identifier: PA2825035316
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 852277
ClinVar RCV Id: RCV001056850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2391Val
CA382559557
NM_000051.4:c.7172C>T