Canonical Allele Identifier: PA194162
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186210
ClinVar RCV Id: RCV000165761 RCV000229485 RCV000235409 RCV001196993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile238Val
CA194160
NM_000051.4:c.712A>G