Canonical Allele Identifier: PA2826636160
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505480
ClinVar RCV Id: RCV002035761 RCV003234796 RCV003493904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp501His
CA346753955
NM_001281494.2:c.1501G>C