Canonical Allele Identifier: PA112608
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 430258
ClinVar RCV Id: RCV000493312 RCV000801338
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Gly217Ser
CA613437
NM_007272.3:c.649G>A