Canonical Allele Identifier: PA108625
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10327
ClinVar RCV Id: RCV000011040 RCV000851849 RCV003114185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Trp2248Cys
CA255218
NM_000132.4:c.6744G>T
CA414904744
NM_000132.4:c.6744G>C