Allele Registry

Canonical Allele Identifier: PA092880

Gene: GRHL2 HGNC NCBI

ClinVar RCV:

RCV000144237

RCV001281606

ClinVar Variation:

156216

HGVS (amino-acid)	Matching Registered Transcripts
NP_079191.2:p.Tyr398His	CA170787 NM_024915.4:c.1192T>C