Canonical Allele Identifier: PA2573165240
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1891Ile
CA389034717
NM_000257.4:c.5672C>T