Canonical Allele Identifier: PA338162
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216227
ClinVar RCV Id: RCV000198750 RCV001025616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2253Gln
CA338160
NM_000051.4:c.6757A>C