Canonical Allele Identifier: PA2826634652
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 420795
ClinVar RCV Id: RCV000484895 RCV000559790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val148Ala
CA16617648
NM_001281494.2:c.443T>C