Canonical Allele Identifier: PA1139668315
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 880650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Arg469Lys
CA7060741
NM_000504.4:c.1406G>A