Canonical Allele Identifier: PA658825433
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 555640
ClinVar RCV Id: RCV000671498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Gly391Arg
CA358941655
NM_000128.4:c.1171G>A
CA358941662
NM_000128.4:c.1171G>C