Allele Registry

Canonical Allele Identifier: PA658749571

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000584693

RCV000587024

RCV000610333

RCV000629874

RCV002828723

RCV004002353

ClinVar Variation:

491954

2008580

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met1202Leu	CA346760557 NM_000179.3:c.3604A>C CA346760558 NM_000179.3:c.3604A>T