Canonical Allele Identifier: PA2826629617
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser28Leu
CA346741097
NM_001281493.2:c.83C>T