Canonical Allele Identifier: PA2573162022
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1676751
ClinVar RCV Id: RCV002222148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ile618Val
CA358946294
NM_000128.4:c.1852A>G