Canonical Allele Identifier: PA2825031168
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2137237
ClinVar RCV Id: RCV003037428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu542Trp
CA228391746
NM_000051.4:c.1625T>G