Canonical Allele Identifier: PA645503244
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407504
ClinVar RCV Id: RCV000467672 RCV000567955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1859Ile
CA16613384
NM_000051.4:c.5576G>T