Canonical Allele Identifier: PA916012011
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233132
ClinVar RCV Id: RCV000220063 RCV000808376 RCV003998031
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp879Gly
CA10578149
NM_001281494.2:c.2636A>G