Canonical Allele Identifier: PA2826348320
Gene: SPIB HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230929.2:p.Arg179Ser
CA406993381
NM_001244000.2:c.535C>A