Canonical Allele Identifier: PA2828473155
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 551946
ClinVar RCV Id: RCV000667122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361014.1:p.Lys350del
CA65811806
NM_001374085.1:c.1048_1050del