Canonical Allele Identifier: PA645386085
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429873
ClinVar RCV Id: RCV000493815 RCV002489212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Gln21Leu
CA223643387
NM_001122955.4:c.62A>T