Canonical Allele Identifier: PA2499230396
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171386
ClinVar RCV Id: RCV001524457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1037Cys
CA389045509
NM_000257.4:c.3110C>G