Canonical Allele Identifier: PA2825048594
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091386
ClinVar RCV Id: RCV004385772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Val38Phe
CA358957914
NM_000128.4:c.112G>T