Canonical Allele Identifier: PA2826441120
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 423549
ClinVar RCV Id: RCV000480400
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244272.1:p.Leu280Phe
CA16617468
NM_001257343.2:c.838C>T