Canonical Allele Identifier: PA2825030394
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2705979
ClinVar RCV Id: RCV003501206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu205Ser
CA382528230
NM_000051.4:c.614T>C