Canonical Allele Identifier: PA1139671756
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 835570
ClinVar RCV Id: RCV001036483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala229Thr
CA389052261
NM_000257.4:c.685G>A