Canonical Allele Identifier: PA645501638
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230299
ClinVar RCV Id: RCV000215026 RCV000460107 RCV000481643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1097Leu
CA10579095
NM_000051.4:c.3291C>G
CA382517261
NM_000051.4:c.3289T>C
CA382517277
NM_000051.4:c.3291C>A