Canonical Allele Identifier: PA2573166252
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys206Gln
CA389052418
NM_000257.4:c.616A>C