Canonical Allele Identifier: PA1139669363
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 989864
ClinVar RCV Id: RCV001277766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Arg284Ser
CA3163795
NM_000128.4:c.852G>C
CA358937393
NM_000128.4:c.852G>T