Canonical Allele Identifier: PA645501207
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236693
ClinVar RCV Id: RCV000228851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe897Leu
CA6265097
NM_000051.4:c.2689T>C
CA10582806
NM_000051.4:c.2691C>G
CA382545187
NM_000051.4:c.2691C>A