Canonical Allele Identifier: PA112636
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 292914
ClinVar RCV Id: RCV000347906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Val235Ile
CA613447
NM_007272.3:c.703G>A