Canonical Allele Identifier: PA2573062021
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1634Ser
CA389037393
NM_000257.4:c.4900C>A