Canonical Allele Identifier: PA916032257
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 821466
ClinVar RCV Id: RCV001015915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val849Met
CA382543673
NM_001351834.2:c.2545G>A