Canonical Allele Identifier: PA2825203323
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091380
ClinVar RCV Id: RCV004385766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Lys410Gln
CA388793789
NM_000504.4:c.1228A>C