Canonical Allele Identifier: PA2827675713
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427936
ClinVar RCV Id: RCV000490913 RCV000515485 RCV001034541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339684.2:p.Pro520Leu
CA350957057
NM_001352755.2:c.1559C>T