Canonical Allele Identifier: PA105444
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10237
ClinVar RCV Id: RCV000010950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asn631Ser
CA255130
NM_000132.4:c.1892A>G