Allele Registry

Canonical Allele Identifier: PA645379360

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000481708

RCV000564150

RCV000697119

ClinVar Variation:

418643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala342Val	CA067043 NM_000179.3:c.1025C>T