Canonical Allele Identifier: PA2826636317
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp537His
CA346754328
NM_001281494.2:c.1609G>C