Canonical Allele Identifier: PA108015
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10147
ClinVar RCV Id: RCV000010860
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro2319Ser
CA255041
NM_000132.4:c.6955C>T