Canonical Allele Identifier: PA658812222
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 517451
ClinVar RCV Id: RCV000604920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Arg1391Cys
CA7528124
NM_153700.2:c.4171C>T