Canonical Allele Identifier: PA2828488029
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214166
ClinVar RCV Id: RCV000199842 RCV003226245 RCV003474949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358373.1:p.Arg109Trp
CA324385
NM_001371444.1:c.325C>T