Canonical Allele Identifier: PA2825413266
Gene: CRTC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161762
ClinVar RCV Id: RCV000149298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036039.1:p.Arg463Ser
CA174738
NM_001042574.3:c.1387C>A