Allele Registry

Canonical Allele Identifier: PA164046

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000114750

RCV000129248

RCV003593911

ClinVar Variation:

126891

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser541Arg	CA008929 NM_000179.3:c.1621A>C CA346747078 NM_000179.3:c.1623C>G CA346747082 NM_000179.3:c.1623C>A