Canonical Allele Identifier: PA2826500859
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098449
ClinVar RCV Id: RCV001420381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Ser369Leu
CA388787171
NM_001267554.1:c.1106C>T