Allele Registry

Canonical Allele Identifier: PA2826635847

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000629678

RCV000774601

RCV001041663

RCV004002769

ClinVar Variation:

525592

839817

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr425Ser	CA068566 NM_001281494.2:c.1274C>G CA346751208 NM_001281494.2:c.1273A>T