Canonical Allele Identifier: PA286734
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127339
ClinVar RCV Id: RCV000115143 RCV000211963 RCV000168231 RCV000515225 RCV003237336 RCV001818258 RCV004549539 RCV003149791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly506Cys
CA286732
NM_000051.4:c.1516G>T