Canonical Allele Identifier: PA645503665
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233776
ClinVar RCV Id: RCV000221486 RCV000533728 RCV001174836 RCV003227722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2113Ser
CA6265906
NM_000051.4:c.6338C>G
CA382552309
NM_000051.4:c.6337A>T