Canonical Allele Identifier: PA183363
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 178947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp928Ala
CA013057
NM_000257.4:c.2783A>C