Canonical Allele Identifier: PA658749767
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490008
ClinVar RCV Id: RCV000579922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe1222Leu
CA346760838
NM_000179.3:c.3664T>C
CA346760843
NM_000179.3:c.3666T>A
CA346760844
NM_000179.3:c.3666T>G