Canonical Allele Identifier: PA112597
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 420177
ClinVar RCV Id: RCV000483666 RCV001856839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Gly217Arg
CA16616982
NM_007272.3:c.649G>C