Canonical Allele Identifier: PA916028528
Gene: GRHL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 505419
ClinVar RCV Id: RCV000610408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317522.1:p.Leu91Met
CA182748622
NM_001330593.2:c.271T>A