Allele Registry

Canonical Allele Identifier: PA916011059

Gene: MSH6 HGNC NCBI

ClinVar Allele:

133024

ClinVar RCV:

RCV000214011

RCV000759850

RCV001041141

RCV003997239

RCV004528799

ClinVar Variation:

127567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ala64Pro	CA009439 NM_001281492.2:c.190G>C