Canonical Allele Identifier: PA2827081800
Gene: TRIP11 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Ser431Leu
CA7313966
NM_001321851.1:c.1292C>T