Allele Registry

Canonical Allele Identifier: PA287308

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

133039

1785502

ClinVar RCV:

RCV000168205

RCV000567226

RCV000656897

RCV000662609

RCV002324752

RCV003997247

ClinVar Variation:

127582

1729213

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val1078Leu	CA012092 NM_000179.3:c.3232G>C CA346758051 NM_000179.3:c.3232G>T