Canonical Allele Identifier: PA2828488481
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6163
ClinVar RCV Id: RCV000006538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358375.1:p.Ser277Asn
CA117984
NM_001371446.1:c.830G>A