Allele Registry

Canonical Allele Identifier: PA2573192684

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001993900

ClinVar Variation:

1469431

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu891Asp	CA346760509 NM_001281494.2:c.2673A>C CA346760510 NM_001281494.2:c.2673A>T