Canonical Allele Identifier: PA915958200
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 627095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Met1874Thr
CA1233452
NM_000130.5:c.5621T>C