Canonical Allele Identifier: PA645486877
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 387667
ClinVar RCV Id: RCV000432216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004319.1:p.Ala242Gly
CA16604137
NM_004328.5:c.725C>G