Canonical Allele Identifier: PA2826636433
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455210
ClinVar RCV Id: RCV000526734 RCV000567854 RCV004003680
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val565Ile
CA069233
NM_001281494.2:c.1693G>A