Canonical Allele Identifier: PA916011539
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly6Asp
CA346740744
NM_001281494.2:c.17G>A