Canonical Allele Identifier: PA2830099938
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149355.1:p.Thr189Met
CA254662
NM_033165.4:c.566C>T