Canonical Allele Identifier: PA1139674466
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924818
ClinVar RCV Id: RCV001186405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile669Val
CA068352
NM_000179.3:c.2005A>G