Canonical Allele Identifier: PA2829672338
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 2983107
ClinVar RCV Id: RCV003847722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Val251_Tyr252insAsnThrArgLysLysProValLeu
CA521458357
NM_007272.3:c.753_754insAACACCCGCAAGAAGCCGGTACTC