Allele Registry

Canonical Allele Identifier: PA2826630624

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000575004

ClinVar Variation:

485855

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile268Leu	CA346748557 NM_001281493.2:c.802A>C CA346748563 NM_001281493.2:c.802A>T