Canonical Allele Identifier: PA2829907282
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10327
ClinVar RCV Id: RCV000011040 RCV000851849 RCV003114185
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Trp113Cys
CA255218
NM_019863.3:c.339G>T
CA414904744
NM_019863.3:c.339G>C