Canonical Allele Identifier: PA111318
Gene: BFSP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 6583
ClinVar RCV Id: RCV000006961 RCV000056969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003562.1:p.Arg287Trp
CA118356
NM_003571.4:c.859C>T