Canonical Allele Identifier: PA286755
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127348
ClinVar RCV Id: RCV000115153 RCV000195938 RCV000589935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn778Ser
CA286753
NM_000051.4:c.2333A>G