Canonical Allele Identifier: PA1139673711
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 870090
ClinVar RCV Id: RCV001089630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1021Ile
CA389045741
NM_000257.4:c.3062C>T