Allele Registry

Canonical Allele Identifier: PA916070932

Gene: SIX5 HGNC NCBI

ClinVar RCV:

RCV000009132

RCV001851753

ClinVar Variation:

8601

HGVS (amino-acid)	Matching Registered Transcripts
NP_787071.3:p.Thr552Met	CA340801 NM_175875.5:c.1655C>T