Canonical Allele Identifier: PA2826626841
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525817
ClinVar RCV Id: RCV000630145 RCV003465388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp567His
CA346750852
NM_001281492.2:c.1699G>C