Allele Registry

Canonical Allele Identifier: PA2826636606

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003278532

ClinVar Variation:

2567491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu603Ser	CA346755343 NM_001281494.2:c.1808T>C