Canonical Allele Identifier: PA2826630047
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 183760
ClinVar RCV Id: RCV000162486 RCV000479506 RCV000500646 RCV000553513 RCV000582500 RCV003454393 RCV003995199 RCV004525833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe130Ser
CA008453
NM_001281493.2:c.389T>C