Canonical Allele Identifier: PA658812194
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 506243
ClinVar RCV Id: RCV000600268 RCV003480713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Ser332Cys
CA392184527
NM_153700.2:c.995C>G