Allele Registry

Canonical Allele Identifier: PA2826348270

Gene: SPIB HGNC NCBI

ClinVar Allele:

2299567

ClinVar RCV:

RCV004154898

ClinVar Variation:

2304610

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230927.1:p.Arg119Ser	CA406993381 NM_001243998.2:c.355C>A