Canonical Allele Identifier: PA2573163069
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser242Asn
CA346740017
NM_000179.3:c.725G>A