Allele Registry

Canonical Allele Identifier: PA645378201

Gene: MSH6 HGNC NCBI

ClinVar Allele:

392813

ClinVar RCV:

RCV000461408

RCV000480657

RCV000573037

RCV000765675

RCV001192488

RCV003463931

ClinVar Variation:

410435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala35Val	CA067076 NM_000179.3:c.104C>T