Canonical Allele Identifier: PA2580346146
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760856
ClinVar RCV Id: RCV002412169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Trp261Cys
CA613471
NM_007272.3:c.783G>T
CA338568044
NM_007272.3:c.783G>C