Canonical Allele Identifier: PA2580346138
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759932
ClinVar RCV Id: RCV002396350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Val255Met
CA18253843
NM_007272.3:c.763G>A