Canonical Allele Identifier: PA2828488728
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214159
ClinVar RCV Id: RCV000200623 RCV000714568 RCV001137963 RCV001137961 RCV000949252 RCV001137962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358376.1:p.Val205Ile
CA325212
NM_001371447.1:c.613G>A