Canonical Allele Identifier: PA913196641
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 618055
ClinVar RCV Id: RCV000756004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Val251Ala
CA338567904
NM_007272.3:c.752T>C