Allele Registry

Canonical Allele Identifier: PA658802214

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000629678

RCV000774601

RCV001041663

RCV004002769

ClinVar Variation:

525592

839817

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr727Ser	CA068566 NM_000179.3:c.2180C>G CA346751208 NM_000179.3:c.2179A>T