Allele Registry

Canonical Allele Identifier: PA178048

Gene: STRC HGNC NCBI

ClinVar RCV:

RCV000151947

RCV000770970

RCV003480064

ClinVar Variation:

165308

HGVS (amino-acid)	Matching Registered Transcripts
NP_714544.1:p.Trp1475Cys	CA178047 NM_153700.2:c.4425G>C CA392166606 NM_153700.2:c.4425G>T