Canonical Allele Identifier: PA2825034932
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826547
ClinVar RCV Id: RCV001025520 RCV001243705 RCV003315445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2224_Arg2227delinsIleSer
CA915947667
NM_000051.4:c.6672_6680delinsCTC