Canonical Allele Identifier: PA1139671739
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 955436
ClinVar RCV Id: RCV001228077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu216Pro
CA389052339
NM_000257.4:c.647T>C