Allele Registry

Canonical Allele Identifier: PA658802441

Gene: MSH6 HGNC NCBI

ClinVar Allele:

518465

ClinVar RCV:

RCV000630015

RCV000771661

RCV003332215

RCV004002789

ClinVar Variation:

525751

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro1086Ser	CA346758131 NM_000179.3:c.3256C>T