Canonical Allele Identifier: PA645294383
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 311227
ClinVar RCV Id: RCV000306848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.Phe313Leu
CA7060190
NM_019616.4:c.937T>C
CA388786154
NM_019616.4:c.939C>A
CA388786155
NM_019616.4:c.939C>G