Canonical Allele Identifier: PA658819689
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 528771
ClinVar RCV Id: RCV000633997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Gln223His
CA613438
NM_007272.3:c.669G>C
CA338567731
NM_007272.3:c.669G>T