Canonical Allele Identifier: PA2499276062
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1163727
ClinVar RCV Id: RCV001509021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Leu220Val
CA338567704
NM_007272.3:c.658C>G