Canonical Allele Identifier: PA2828489100
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 423549
ClinVar RCV Id: RCV000480400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358377.1:p.Leu280Phe
CA16617468
NM_001371448.1:c.838C>T