Canonical Allele Identifier: PA2828487771
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214161
ClinVar RCV Id: RCV000198924 RCV001833143 RCV002492899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358372.1:p.Val167Met
CA323457
NM_001371443.1:c.499G>A