Canonical Allele Identifier: PA2826440802
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214166
ClinVar RCV Id: RCV000199842 RCV003226245 RCV003474949
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244272.1:p.Arg109Trp
CA324385
NM_001257343.2:c.325C>T