Canonical Allele Identifier: PA1139670075
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 883022
ClinVar RCV Id: RCV001113154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Leu461Pro
CA388787213
NM_000131.4:c.1382T>C