Canonical Allele Identifier: PA916011127
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216321
ClinVar RCV Id: RCV000197162 RCV000220344 RCV000582427 RCV000761118 RCV000663025 RCV001699153 RCV003468905
ClinVar Variation Id: 958041
ClinVar RCV Id: RCV001231129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val85Ile
CA073285
NM_001281492.2:c.253G>A
CA1139657002
NM_001281492.2:c.252_253delinsTA