Allele Registry

Canonical Allele Identifier: PA2826630300

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003026792

ClinVar Variation:

2107070

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ala192Gly	CA346746045 NM_001281493.2:c.575C>G