Allele Registry

Canonical Allele Identifier: PA2826625701

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

182063

ClinVar RCV:

RCV000162486

RCV000479506

RCV000500646

RCV000553513

RCV000582500

RCV003454393

RCV003995199

RCV004525833

ClinVar Variation:

183760

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe302Ser	CA008453 NM_001281492.2:c.905T>C