Canonical Allele Identifier: PA658680270
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483843
ClinVar Variation Id: 483876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser242Arg
CA346740014
NM_000179.3:c.724A>C
CA346740020
NM_000179.3:c.726C>A
CA346740022
NM_000179.3:c.726C>G