Canonical Allele Identifier: PA2826632140
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455218
ClinVar RCV Id: RCV000549264 RCV002438283
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu617Lys
CA346755427
NM_001281493.2:c.1849G>A