Canonical Allele Identifier: PA2826629729
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421018
ClinVar RCV Id: RCV000485837 RCV000582356 RCV000629703 RCV003464014 RCV004003341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp55Asn
CA067106
NM_001281493.2:c.163G>A