Canonical Allele Identifier: PA916033608
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482620
ClinVar RCV Id: RCV000563451 RCV000806909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met1909Ile
CA382547952
NM_001351834.2:c.5727G>A
CA382547953
NM_001351834.2:c.5727G>C
CA382547954
NM_001351834.2:c.5727G>T