Canonical Allele Identifier: PA104412
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 420160
ClinVar RCV Id: RCV000482463 RCV001095705 RCV003313784
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Thr384Met
CA7060229
NM_000131.4:c.1151C>T