Canonical Allele Identifier: PA2741815800
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2572129
ClinVar RCV Id: RCV003313867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Arg346Cys
CA7060670
NM_000504.4:c.1036C>T