Canonical Allele Identifier: PA915977823
Gene: TMEM132C HGNC NCBI

Linked Data

ClinVar Variation Id: 776778
ClinVar RCV Id: RCV000957152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129575.2:p.Val232Met
CA6874509
NM_001136103.3:c.694G>A