Canonical Allele Identifier: PA2826636871
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821967
ClinVar RCV Id: RCV001016915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile665Ser
CA915943938
NM_001281494.2:c.1994_1995delinsGT