Canonical Allele Identifier: PA2829704624
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 3226056
ClinVar RCV Id: RCV004517326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Thr58Ala
CA338565026
NM_007272.3:c.172A>G