Canonical Allele Identifier: PA2825030932
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1463295
ClinVar RCV Id: RCV001956597
ClinVar Variation Id: 2010709
ClinVar RCV Id: RCV002834193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met437Leu
CA382533628
NM_000051.4:c.1309A>C
CA382533631
NM_000051.4:c.1309A>T