Allele Registry

Canonical Allele Identifier: PA165397

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129947

RCV000502711

RCV000629697

RCV001582602

RCV003997536

ClinVar Variation:

141434

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu952Pro	CA011015 NM_000179.3:c.2855T>C