Canonical Allele Identifier: PA2826440305
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1423511
ClinVar RCV Id: RCV001954819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244271.1:p.Arg224His
CA2109727
NM_001257342.2:c.671G>A