Canonical Allele Identifier: PA891850484
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 568567
ClinVar RCV Id: RCV000688965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Arg254Gln
CA613463
NM_007272.3:c.761G>A