Canonical Allele Identifier: PA168419
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142460
ClinVar RCV Id: RCV000131592 RCV000692438 RCV001193604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2240His
CA168417
NM_000051.4:c.6718G>C