Allele Registry

Canonical Allele Identifier: PA2573061728

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001753358

RCV001868750

ClinVar Variation:

1318811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe461Ser	CA346745004 NM_000179.3:c.1382T>C