Canonical Allele Identifier: PA2573162390
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685785
ClinVar RCV Id: RCV002249952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Met1992Ile
CA10567922
NM_000132.4:c.5976G>A
CA414905559
NM_000132.4:c.5976G>T
CA414905561
NM_000132.4:c.5976G>C