Canonical Allele Identifier: PA2741899287
Gene: THBS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003238.2:p.Asn993Ser
CA366458091
NM_003247.4:c.2978A>G