Canonical Allele Identifier: PA2825035956
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2419994
ClinVar RCV Id: RCV003118519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2684His
CA6266268
NM_000051.4:c.8052G>C
CA382561929
NM_000051.4:c.8052G>T