Canonical Allele Identifier: PA916032001
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489521
ClinVar RCV Id: RCV000580002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met660Val
CA382536861
NM_001351834.2:c.1978A>G