Canonical Allele Identifier: PA107260
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10127
ClinVar RCV Id: RCV000010840
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Leu2185Ser
CA255028
NM_000132.4:c.6554T>C