Canonical Allele Identifier: PA296818
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181341
ClinVar RCV Id: RCV001704142 RCV002466453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met439Val
CA010515
NM_000257.4:c.1315A>G