Canonical Allele Identifier: PA645464750
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 292905
ClinVar RCV Id: RCV000363743
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Ser16Gly
CA613199
NM_007272.3:c.46A>G