Canonical Allele Identifier: PA2826726101
Gene: ARMC12 HGNC NCBI

Linked Data

ClinVar Variation Id: 161808
ClinVar RCV Id: RCV000149344
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273505.1:p.Asp201Tyr
CA174824
NM_001286576.2:c.601G>T