Canonical Allele Identifier: PA174420
Gene: MYH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161597
ClinVar RCV Id: RCV000149133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002463.2:p.Arg780Ile
CA174419
NM_002472.3:c.2339G>T