Allele Registry

Canonical Allele Identifier: PA163997

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129223

RCV000204246

RCV001775618

RCV003997487

ClinVar Variation:

140947

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1354Pro	CA015365 NM_000179.3:c.4061T>C