Canonical Allele Identifier: PA916031999
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407501
ClinVar RCV Id: RCV000474729 RCV000564798 RCV003493577
ClinVar Variation Id: 937882
ClinVar RCV Id: RCV001207000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys659Asn
CA16613349
NM_001351834.2:c.1977G>T
CA382536859
NM_001351834.2:c.1977G>C