Canonical Allele Identifier: PA2828880963
Gene: THBS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368871.1:p.Asn916Ser
CA366458091
NM_001381942.1:c.2747A>G