Canonical Allele Identifier: PA2825588141
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738621
ClinVar RCV Id: RCV003581506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Tyr277Ser
CA380962046
NM_001122955.4:c.830A>C