Canonical Allele Identifier: PA193987
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186146
ClinVar RCV Id: RCV000165684 RCV000628179 RCV000844955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys1964Asn
CA193985
NM_000051.4:c.5892G>C
CA382548548
NM_000051.4:c.5892G>T