Canonical Allele Identifier: PA356388
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 220775
ClinVar RCV Id: RCV000206762 RCV000478981 RCV000573505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1296Ser
CA350768
NM_000051.4:c.3886C>T