Canonical Allele Identifier: PA2825033998
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1023271
ClinVar RCV Id: RCV001323288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1803His
CA382543783
NM_000051.4:c.5407G>C