Canonical Allele Identifier: PA658801191
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524285
ClinVar RCV Id: RCV000627947 RCV002420658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp661Asn
CA228393576
NM_000051.4:c.1981G>A