Canonical Allele Identifier: PA645414721
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr265Asn
CA10581179
NM_000257.4:c.794C>A