Canonical Allele Identifier: PA2499299583
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1012670
ClinVar RCV Id: RCV001310748 RCV004017818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Thr1565Ser
CA7527945
NM_153700.2:c.4693A>T
CA392163405
NM_153700.2:c.4694C>G