Canonical Allele Identifier: PA346508
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 180433
ClinVar RCV Id: RCV000157352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr265Ser
CA016835
NM_000257.4:c.793A>T
CA389052039
NM_000257.4:c.794C>G