Canonical Allele Identifier: PA645464774
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 240766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Glu225Ala
CA613439
NM_007272.3:c.674A>C