Canonical Allele Identifier: PA296682
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181263
ClinVar RCV Id: RCV000526209 RCV001184264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1563Val
CA015233
NM_000257.4:c.4687C>G