Canonical Allele Identifier: PA2825203252
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098480
ClinVar RCV Id: RCV001420412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Arg28Ser
CA388787421
NM_000504.4:c.84G>C
CA388787422
NM_000504.4:c.84G>T