Canonical Allele Identifier: PA658743056
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490628
ClinVar RCV Id: RCV000584470 RCV000812625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1966Asn
CA382548560
NM_000051.4:c.5897G>A