Allele Registry

Canonical Allele Identifier: PA2826629899

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002003501

ClinVar Variation:

1486313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu94Phe	CA346742399 NM_001281493.2:c.280C>T