Canonical Allele Identifier: PA108258
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 439683
ClinVar RCV Id: RCV000851606 RCV002248743 RCV003103799 RCV002476015 RCV001267618 RCV001803794
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser2030Asn
CA10567911
NM_000132.4:c.6089G>A