Canonical Allele Identifier: PA915991518
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 826915
ClinVar RCV Id: RCV001229055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009203.2:p.Arg241Trp
CA613453
NM_007272.3:c.721C>T