Canonical Allele Identifier: PA2825035836
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2807738
ClinVar RCV Id: RCV003606115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2626Gly
CA382561426
NM_000051.4:c.7877C>G