Canonical Allele Identifier: PA2741810068
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577222
ClinVar RCV Id: RCV003324299 RCV003561299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ala430Ser
CA358942244
NM_000128.4:c.1288G>T