Allele Registry

Canonical Allele Identifier: PA658680771

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000564992

RCV003451218

ClinVar Variation:

479958

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu637Pro	CA346750185 NM_000179.3:c.1910T>C