Canonical Allele Identifier: PA2829080561
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_001373987.1:p.Val212Met
CA6874509
NM_001387058.1:c.634G>A