Canonical Allele Identifier: PA645501618
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 229707
ClinVar RCV Id: RCV000214272 RCV000671975 RCV001546529 RCV003153495 RCV003468979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met1064Val
CA6265222
NM_000051.4:c.3190A>G