Canonical Allele Identifier: PA658814037
Gene: GRHL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 505419
ClinVar RCV Id: RCV000610408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079191.2:p.Leu107Met
CA182748622
NM_024915.4:c.319T>A