Canonical Allele Identifier: PA915958014
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 627211
ClinVar RCV Id: RCV000851996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Glu379Asp
CA358941480
NM_000128.4:c.1137G>C
CA358941481
NM_000128.4:c.1137G>T