Allele Registry

Canonical Allele Identifier: PA2826626492

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001347523

ClinVar Variation:

1043419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln488Pro	CA346749745 NM_001281492.2:c.1463A>C