Canonical Allele Identifier: PA2828489356
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1423511
ClinVar RCV Id: RCV001954819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358378.1:p.Arg224His
CA2109727
NM_001371449.1:c.671G>A