Canonical Allele Identifier: PA645414698
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp239Glu
CA10581181
NM_000257.4:c.717C>G
CA389052198
NM_000257.4:c.717C>A