Canonical Allele Identifier: PA102840
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ala63Val
CA219136
NM_000128.4:c.188C>T