Canonical Allele Identifier: PA169360
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142768
ClinVar RCV Id: RCV000132161 RCV000203804 RCV000480825 RCV003998134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu484Gln
CA008646
NM_000179.3:c.1450G>C