Canonical Allele Identifier: PA2580346139
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759982
ClinVar RCV Id: RCV002396400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Val255Gly
CA338567942
NM_007272.3:c.764T>G