Canonical Allele Identifier: PA2826726081
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_001273503.1:p.Asp201Tyr
CA174824
NM_001286574.2:c.601G>T