Allele Registry

Canonical Allele Identifier: PA2826632711

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000569620

RCV000795073

ClinVar Variation:

479881

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile752Met	CA070144 NM_001281493.2:c.2256C>G