Canonical Allele Identifier: PA2826630788
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile306Val
CA009270
NM_001281493.2:c.916A>G