Allele Registry

Canonical Allele Identifier: PA645381542

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000221120

RCV000525574

RCV000997142

RCV003462507

RCV003998019

ClinVar Variation:

232999

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp713Asn	CA10578093 NM_000179.3:c.2137G>A