Canonical Allele Identifier: PA2741810154
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2604551
ClinVar RCV Id: RCV003343269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Thr405Ser
CA343128538
NM_000130.5:c.1214C>G
CA343128544
NM_000130.5:c.1213A>T