Allele Registry

Canonical Allele Identifier: PA2826630306

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001011829

ClinVar Variation:

819349

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Cys194Ser	CA346746068 NM_001281493.2:c.580T>A CA346746071 NM_001281493.2:c.581G>C