Canonical Allele Identifier: PA2826633576
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232375
ClinVar RCV Id: RCV000218524 RCV001243869 RCV003462494 RCV003322762 RCV003997965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg940Cys
CA10578156
NM_001281493.2:c.2818C>T