Canonical Allele Identifier: PA916011044
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 202200
ClinVar RCV Id: RCV000184046 RCV000582619 RCV000630169 RCV001420817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro59Thr
CA009135
NM_001281492.2:c.175C>A