Allele Registry

Canonical Allele Identifier: PA2826630840

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001347523

ClinVar Variation:

1043419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln316Pro	CA346749745 NM_001281493.2:c.947A>C