Canonical Allele Identifier: PA1139668331
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 880651
ClinVar RCV Id: RCV001109103 RCV004032141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Pro472Leu
CA388794611
NM_000504.4:c.1415C>T