Canonical Allele Identifier: PA658802087
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524404
ClinVar RCV Id: RCV000628170 RCV001188329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2797Asn
CA382516614
NM_000051.4:c.8390G>A