Canonical Allele Identifier: PA2828489665
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2177843
ClinVar RCV Id: RCV002595304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358379.1:p.Arg224Cys
CA350627929
NM_001371450.1:c.670C>T