Canonical Allele Identifier: PA645294918
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 285379
ClinVar RCV Id: RCV000352684 RCV000725651 RCV001828215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Gly478Arg
CA3163979
NM_000128.4:c.1432G>A
CA358943562
NM_000128.4:c.1432G>C