Allele Registry

Canonical Allele Identifier: PA658812222

Gene: STRC HGNC NCBI

ClinVar RCV:

RCV000604920

ClinVar Variation:

517451

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