Canonical Allele Identifier: PA2825031859
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1424880
ClinVar RCV Id: RCV001924107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln852His
CA382543772
NM_000051.4:c.2556G>T
CA382543774
NM_000051.4:c.2556G>C