Allele Registry

Canonical Allele Identifier: PA2825088767

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004013960

ClinVar Variation:

3074426

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys603Asn	CA346749377 NM_000179.3:c.1809G>C CA346749378 NM_000179.3:c.1809G>T