Canonical Allele Identifier: PA2826633562
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644095
ClinVar RCV Id: RCV000797936
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile937Met
CA346761011
NM_001281493.2:c.2811A>G