Allele Registry

Canonical Allele Identifier: PA3057502365

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV005106332

ClinVar Variation:

3633927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro160Ser	CA346745022 NM_001281494.2:c.478C>T