Canonical Allele Identifier: PA2828472707
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1120065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361014.1:p.Ser65Arg
CA2109617
NM_001374085.1:c.193A>C
CA350625828
NM_001374085.1:c.195C>A
CA350625829
NM_001374085.1:c.195C>G