Canonical Allele Identifier: PA2826607938
Gene: BFSP1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265536.1:p.Thr537Ile
CA9771947
NM_001278607.2:c.1610C>T