Canonical Allele Identifier: PA2827054574
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307646.1:p.Pro99Leu
CA117989
NM_001320717.2:c.296C>T