Canonical Allele Identifier: PA2826634275
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro18Leu
CA073651
NM_001281494.2:c.53C>T