Canonical Allele Identifier: PA174825
Gene: ARMC12 HGNC NCBI

Linked Data

ClinVar Variation Id: 161808
ClinVar RCV Id: RCV000149344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659465.2:p.Asp228Tyr
CA174824
NM_145028.5:c.682G>T