Allele Registry

Canonical Allele Identifier: PA658802132

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000629901

RCV002404726

ClinVar Variation:

525697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe569Leu	CA346748540 NM_000179.3:c.1705T>C CA346748550 NM_000179.3:c.1707C>A CA346748554 NM_000179.3:c.1707C>G