Canonical Allele Identifier: PA2826441054
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2178063
ClinVar RCV Id: RCV002588500
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244272.1:p.Leu243Val
CA350629735
NM_001257343.2:c.727C>G