Canonical Allele Identifier: PA182501
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 178529
ClinVar RCV Id: RCV000155277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Glu1727Gln
CA182500
NM_153700.2:c.5179G>C