Canonical Allele Identifier: PA286968
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127437
ClinVar RCV Id: RCV000115242 RCV000494662 RCV000534806 RCV001171474 RCV003467031 RCV002483185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2394Leu
CA286966
NM_000051.4:c.7181C>T