Canonical Allele Identifier: PA1139672710
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 951825
ClinVar RCV Id: RCV001223820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser315Phe
CA46707062
NM_000179.3:c.944C>T