Canonical Allele Identifier: PA2828880789
Gene: THBS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368868.1:p.Asn935Ser
CA366458091
NM_001381939.1:c.2804A>G