Canonical Allele Identifier: PA195206
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186571
ClinVar RCV Id: RCV000166188 RCV001234206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys2286Tyr
CA195204
NM_000051.4:c.6857G>A