Allele Registry

Canonical Allele Identifier: PA2826636801

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129947

RCV000502711

RCV000629697

RCV001582602

RCV003997536

ClinVar Variation:

141434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu650Pro	CA011015 NM_001281494.2:c.1949T>C