Canonical Allele Identifier: PA1139670030
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 988831
ClinVar RCV Id: RCV001270525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Ala286Val
CA7060149
NM_000131.4:c.857C>T