Canonical Allele Identifier: PA2830333623
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 3171608
ClinVar RCV Id: RCV004458479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Arg1577Trp
CA7527915
NM_153700.2:c.4729C>T