Canonical Allele Identifier: PA2827675713
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427936

Amino-acid Alleles

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