Canonical Allele Identifier: PA112562
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 8178
ClinVar RCV Id: RCV000008657 RCV000119045 RCV002247276 RCV003421912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Arg254Trp
CA119351
NM_007272.3:c.760C>T