Canonical Allele Identifier: PA108000
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10332
ClinVar RCV Id: RCV000011045 RCV000851613 RCV001701721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro2319Leu
CA255224
NM_000132.4:c.6956C>T