Canonical Allele Identifier: PA2826635699
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 936576
ClinVar RCV Id: RCV001205404
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys390Asn
CA346750807
NM_001281494.2:c.1170A>C
CA346750808
NM_001281494.2:c.1170A>T