Canonical Allele Identifier: PA1139743100
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214159
ClinVar RCV Id: RCV000200623 RCV000714568 RCV001137963 RCV001137961 RCV000949252 RCV001137962
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358380.1:p.Val85Ile
CA325212
NM_001371451.1:c.253G>A