Canonical Allele Identifier: PA2826636598
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127573
ClinVar RCV Id: RCV000115394 RCV000535809 RCV000583327 RCV003997242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp602Glu
CA010773
NM_001281494.2:c.1806T>G
CA346755341
NM_001281494.2:c.1806T>A