Canonical Allele Identifier: PA131751
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42844
ClinVar RCV Id: RCV000035724 RCV000804896 RCV000852456 RCV003313931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp469Tyr
CA010710
NM_000257.4:c.1405G>T