Canonical Allele Identifier: PA916032002
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481260
ClinVar RCV Id: RCV000564336 RCV000628031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met660Thr
CA382536867
NM_001351834.2:c.1979T>C