Canonical Allele Identifier: PA645503096
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236730
ClinVar RCV Id: RCV000233443 RCV000481313 RCV000579553 RCV003469127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1715Pro
CA6265633
NM_000051.4:c.5144T>C