Canonical Allele Identifier: PA916034118
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 572261
ClinVar RCV Id: RCV000693600 RCV000772397 RCV001356011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Trp2300Gly
CA382556936
NM_001351834.2:c.6898T>G