Canonical Allele Identifier: PA2580346113
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1755131
ClinVar RCV Id: RCV002369160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Leu224Phe
CA338567737
NM_007272.3:c.672G>C
CA338567738
NM_007272.3:c.672G>T