Allele Registry

Canonical Allele Identifier: PA2499229293

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001347523

ClinVar Variation:

1043419

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln618Pro	CA346749745 NM_000179.3:c.1853A>C