Canonical Allele Identifier: PA1139671942
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 923963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile285Val
CA049384
NM_000257.4:c.853A>G