Canonical Allele Identifier: PA2828472722
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 554974
ClinVar RCV Id: RCV000670706 RCV000778591 RCV001171821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361014.1:p.Arg73Cys
CA2109627
NM_001374085.1:c.217C>T