Canonical Allele Identifier: PA2826634604
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769757
ClinVar RCV Id: RCV002385540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met136Ile
CA346744388
NM_001281494.2:c.408G>A
CA346744389
NM_001281494.2:c.408G>C
CA346744390
NM_001281494.2:c.408G>T