Canonical Allele Identifier: PA2826630262
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455138
ClinVar RCV Id: RCV000554233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln183Pro
CA346745731
NM_001281493.2:c.548A>C