Allele Registry

Canonical Allele Identifier: PA2826630925

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000564992

RCV003451218

ClinVar Variation:

479958

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu335Pro	CA346750185 NM_001281493.2:c.1004T>C