Canonical Allele Identifier: PA131973
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42997
ClinVar RCV Id: RCV000035891 RCV004018780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1403Asp
CA014643
NM_000257.4:c.4208C>A