Canonical Allele Identifier: PA645501299
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232475
ClinVar RCV Id: RCV000218308 RCV001041990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser934Arg
CA10579070
NM_000051.4:c.2802C>G
CA382545660
NM_000051.4:c.2800A>C
CA382545671
NM_000051.4:c.2802C>A