Canonical Allele Identifier: PA2825034933
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1501968
ClinVar RCV Id: RCV002010861 RCV002361380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2224Ile
CA382554867
NM_000051.4:c.6672G>T
CA382554868
NM_000051.4:c.6672G>C
CA382554869
NM_000051.4:c.6672G>A