Canonical Allele Identifier: PA332399
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135830
ClinVar RCV Id: RCV000122952 RCV000219239 RCV000218729 RCV000411179 RCV000524115 RCV000780476 RCV003460868 RCV003492534
ClinVar Variation Id: 1776067
ClinVar RCV Id: RCV002398584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu533Asp
CA008846
NM_000179.3:c.1599G>C
CA346746950
NM_000179.3:c.1599G>T