Canonical Allele Identifier: PA2573078565
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 581808
ClinVar RCV Id: RCV000705740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Val227Phe
CA380963063
NM_001386028.1:c.679G>T