Canonical Allele Identifier: PA2826630372
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233637
ClinVar RCV Id: RCV000221108 RCV000550953 RCV003469083 RCV003998570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile211Val
CA067819
NM_001281493.2:c.631A>G