Canonical Allele Identifier: PA2580346148
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761026
ClinVar RCV Id: RCV002412339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Asn263Thr
CA613473
NM_007272.3:c.788A>C