Canonical Allele Identifier: PA658801524
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524275
ClinVar RCV Id: RCV000627929 RCV001022268 RCV001532956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1437Ser
CA382531713
NM_000051.4:c.4311A>C
CA382531717
NM_000051.4:c.4311A>T