Canonical Allele Identifier: PA192416
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185611
ClinVar RCV Id: RCV000165060 RCV000201982 RCV000410385 RCV000656900 RCV001082754 RCV003323297
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1160Ile
CA013029
NM_000179.3:c.3478G>A