Canonical Allele Identifier: PA645294913
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 348375
ClinVar RCV Id: RCV000308480 RCV000890695 RCV003922528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys339Phe
CA3163834
NM_000128.4:c.1016G>T