Canonical Allele Identifier: PA2573252499
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1441303
ClinVar RCV Id: RCV001979076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Asp260Tyr
CA338568016
NM_007272.3:c.778G>T