Canonical Allele Identifier: PA2580205703
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2007318
ClinVar RCV Id: RCV002842228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2235Ile
CA382554961
NM_001351834.2:c.6705G>A
CA382554964
NM_001351834.2:c.6705G>C
CA382554966
NM_001351834.2:c.6705G>T