Allele Registry

Canonical Allele Identifier: PA658681248

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000569620

RCV000795073

ClinVar Variation:

479881

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile1054Met	CA070144 NM_000179.3:c.3162C>G