Canonical Allele Identifier: PA2580105338
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2363422
ClinVar RCV Id: RCV002990118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Lys1712Asn
CA414913785
NM_000132.4:c.5136G>T
CA414913786
NM_000132.4:c.5136G>C