Canonical Allele Identifier: PA2826632021
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu591Val
CA069423
NM_001281493.2:c.1771C>G