Canonical Allele Identifier: PA645464755
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 292907
ClinVar RCV Id: RCV000305597
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Ala28Thr
CA613211
NM_007272.3:c.82G>A