Canonical Allele Identifier: PA658674075
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482529
ClinVar RCV Id: RCV000561363 RCV001221844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val835Leu
CA6265052
NM_000051.4:c.2503G>T
CA382543327
NM_000051.4:c.2503G>C