Canonical Allele Identifier: PA2825085842
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1727363
ClinVar RCV Id: RCV002319878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr103Asp
CA346736789
NM_000179.3:c.307T>G