Allele Registry

Canonical Allele Identifier: PA132887

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000036624

RCV000148900

RCV000149450

RCV000588568

RCV000755701

RCV000771256

RCV000852592

RCV001081698

RCV001099310

RCV001099311

RCV002433498

ClinVar Variation:

43675

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001430.1:p.Ala28Val	CA004079 NM_001001430.3:c.83C>T