Canonical Allele Identifier: PA916031774
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481333
ClinVar RCV Id: RCV000575362 RCV000813284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu481Phe
CA228391034
NM_001351834.2:c.1443A>C
CA382534084
NM_001351834.2:c.1443A>T