Canonical Allele Identifier: PA658670976
Gene: BFSP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 474094
ClinVar RCV Id: RCV000552880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003562.1:p.Arg318Ser
CA2623412
NM_003571.4:c.954G>T
CA354585848
NM_003571.4:c.954G>C