Canonical Allele Identifier: PA645383794
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233674
ClinVar RCV Id: RCV000214591 RCV001854702 RCV002472974 RCV003998571
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1098Tyr
CA10578139
NM_000179.3:c.3293G>A